| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00821925022928 | 70921877 | ETB | PROSTHESIS, PARTIAL OSSICULAR REPLACEMENT | 2 | FLPL/WR MALL PSTN .8MM X 1MM X 6.75MM | ||
| 2 | 00821925016323 | 130413 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | GOLDMAN BALL PROBE SMALL, 20 DEGREE TIP ANGLE .51 MM TIP DIAMETER STA | ||
| 3 | 00821925022751 | 70921396 | ETA | REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL | 2 | SHEA MALLEUS PSTN L 4.0M X .8M | ||
| 4 | 00821925022706 | 70921376 | EOB | NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID) | 2 | MACHIDA LIGHT SOURCE RECEPTABLE FOR | ||
| 5 | 00821925022591 | 70134009 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | VOCOM IMPLANT INSERTER W/GRIP TIP | ||
| 6 | 00821925022300 | 70921514 | ETD | TUBE, TYMPANOSTOMY | 2 | CLASSIC SS 4MM GLASS BEADED | ||
| 7 | 00821925021969 | 70326131 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | STAPES DIAMOND BURR 2.3MM DIAMETER STAINLESS STEEL (NON-STERILE) | ||
| 8 | 00821925021938 | 70326128 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | STAPES DIAMOND BURR 1.7MM DIAMETER STAINLESS STEEL (NON-STERILE) | ||
| 9 | 00821925021891 | 70327008 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | MASTOID DIAMOND BURR STERILE 4.5 MM DIAMETER X 70 MM LENGTH STAINLESS | ||
| 10 | 00821925021822 | 70327001 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | MASTOID DIAMOND BURR STERILE 1.0MM DIAMETER X 70MM LENGTH STAINLESS S | ||
| 11 | 00821925021747 | 70326120 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | STAPES DIAMOND BURR .5MM DIAMETER STAINLESS STEEL (NON-STERILE) STAIN | ||
| 12 | 00821925021723 | 70326110 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | STAPES ROUND CUTTING BURR 2.0MM DIAMETER STAINLESS STEEL (NON-STERILE | ||
| 13 | 00821925021686 | 7201017 | 7201017 CABLE, RC-20, REUSABLE | GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 2 | SOMNOPLASTY RC20 CABLE REUSABLE FOR USE W/1120, 2220, 2420 | |
| 14 | 00821925021594 | 70142168 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | SMART STAPES PISTON 04MM X 525MM TRIMMABLE TO 35MM NITINOL FLUOROPLASTIC | |
| 15 | 00821925021556 | 70142165 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | RICHARDS BUCKET HANDLE 10 MM WELL ID 6 MM DIA 425 MM LONG TITANIUM | |
| 16 | 00821925021433 | 70921784 | Means of reconstruction of natural or surgically created defects of the mastoid Means of reconstruction of natural or surgically created defects of the mastoid lining the canal wall or the attic of the tympanic cavity | LYC | Bone Grafting Material, Synthetic | 2 | KARTUSH HA DISC 7MM HA | |
| 17 | 00821925021112 | 70326108 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | STAPES ROUND CUTTING BURR 1.7MM DIAMETER STAINLESS STEEL (NON-STERILE | ||
| 18 | 00821925020979 | 70326542 | EQJ | BUR, EAR, NOSE AND THROAT | 1 | MASTOID ROUND CUTTING BURR STERILE 5.5MM DIAMETER X 65MM LENGTH STAIN | ||
| 19 | 00821925020740 | 70140733 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | DE LA CRUZ PISTON 06MM DIA 425MM LENGTH PLATINUMFLUOROPLASTIC | |
| 20 | 00821925020702 | 70140729 | ETA | Replacement, Ossicular Prosthesis, Total | 2 | DE LA CRUZ PISTON 06MM DIA 450MM LENGTH STAINLESS STEELFLUOROPLASTIC | ||
| 21 | 00821925020610 | 70143253 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process. | ETB | Prosthesis, Partial Ossicular Replacement | 2 | DORNHOFFER MICRON FOOTPLATE SHOE FOR USE WITH 9MM TITANIUM SHAFT TITANIUM | |
| 22 | 00821925020511 | 70143652 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | SMART 360 STAPES PISTON 05MM X 425MM NITINOL FLUOROPLASTIC CIRCUMFERENTIAL | |
| 23 | 00821925020153 | 325507 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | SYNERGY HANDPIECE | ||
| 24 | 00821925019911 | 230557 | EOB | NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID) | 2 | RICHARDS SINUSCOPE ADAPTOR FOR LIGHT CABLE | ||
| 25 | 00821925019522 | 231032 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | WEBSTER NEEDLE HOLDER OVERALL LENGTH 15.2CM (6") GLASS BEAD FINISH | ||
| 26 | 00821925019423 | 230061 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | EAR SURGERY SCISSORS STRAIGHT STAINLESS STEEL, EBONY FINISH | ||
| 27 | 00821925019379 | 23-5200 | "23-5200 OTOVIEW SCOPE 1.7MM 0 DEG" | EWA | SET, AUDIOMETER CALIBRATION | 1 | OTOVIEW RIGID ENDOSCOPE 1.7MM, 0 DEGREES NONAUTOCLAVABLE | |
| 28 | 00821925019324 | 143005 | Provide an implant and securing shim to medialize the paralyzed vocal cord | KHJ | Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material) | 2 | VOCOM SHIM 2 MM OFFSET DENSE HYDROXYLAPATITE | |
| 29 | 00821925019249 | 143008 | Provide an implant and securing shim to medialize the paralyzed vocal cord | KHJ | Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material) | 2 | VOCOM IMPLANT 7MM DISPLACEMENT DENSE HYDROXYLAPATITE | |
| 30 | 00821925019232 | 143007 | Provide an implant and securing shim to medialize the paralyzed vocal cord | KHJ | Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material) | 2 | VOCOM SHIM 0 MM OFFSET DENSE HYDROXYLAPATITE | |
| 31 | 00821925019119 | 150180 | ETD | Tube, Tympanostomy | 2 | SHEA FOAM HEAD SUPPORT LARGE NONSTERILE | ||
| 32 | 00821925018976 | 231014 | GUTHRIE HOOK, SMALL, EBONY | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | GUTHRIE HOOK SMALL EBONY FINISH | |
| 33 | 00821925018921 | 131209 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | FINE, CURVED UP 3 MM X .5 MM JAW SHEA OVAL CUP ALLIG. FORCEPS | ||
| 34 | 00821925018884 | 131205 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | CAWTHORNE ALLIGATOR FORCEPS FINE, STRAIGHT, SMOOTH JAW 3 MM X .5 MM J | ||
| 35 | 00821925018785 | 130447 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | MCGEE PICK STRAIGHT STAINLESS STEEL EBONY FINISH | ||
| 36 | 00821925018730 | 140816 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | RICHARDS PISTON 45MM LENGTH 5MM DIAMETER PLATINUM FLUOROPLASTIC | |
| 37 | 00821925018679 | 140794 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | RICHARDS PISTON 45 MM LENGTH 8MM DIAMETER PLATINUM FLUOROPLASTIC | |
| 38 | 00821925018464 | 130436 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | FARRIOR RASP .60 MM TIP DIAMETER STAINLESS STEEL EBONY FINISH | ||
| 39 | 00821925016149 | 140744 | Replace the portion of the ossicular chain that has lost its function due to Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | TRAPEZE RIBBON LOOP 475 MM LENGTH PLATINUM | |
| 40 | 00821925018402 | 140787 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | RICHARDS PISTON 50 MM LENGTH 6MM DIAMETER PLATINUM FLUOROPLASTIC | |
| 41 | 00821925018389 | 140785 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | RICHARDS PISTON 45 MM LENGTH 6MM DIAMETER PLATINUM FLUOROPLASTIC | |
| 42 | 00821925017726 | 140974 | Replace the portion of the ossicular chain that has lost its function due to dis Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process | ETB | Prosthesis, Partial Ossicular Replacement | 2 | APPLEBAUM INCUS REPLACEMENT 35 MM DENSE HYDROXYLAPATITE | |
| 43 | 00821925016026 | 130860 | LRC | INSTRUMENT, ENT MANUAL SURGICAL | 1 | SHEA-ROBERTSON MIRROR MIDDLE-EAR STAINLESS STEEL | ||
| 44 | 00821925017528 | 140115-ENT | ETA | Replacement, Ossicular Prosthesis, Total | 2 | SCHUKNECHT FLUOROPLASTICWIRE MALLEUS ATTACHMENT PISTON 55MM LENGTH 8MM DIAMETER | ||
| 45 | 00821925039476 | CD-B612LA | KNS | Unit, electrosurgical, endoscopic (with or without accessories) | 2 | 10FR FIXEDPIN HEMOSTATIC PROBE | ||
| 46 | 00821925015944 | 140143-ENT | ETA | Replacement, Ossicular Prosthesis, Total | 2 | MCGEE PISTON 375 MM LENGTH 8 MM DIAMETER STAINLESS | ||
| 47 | 00821925045170 | DSD40MMSC | DISP SINUS DEBRIDER, 4MM MALL, STD, SERRATED | ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Celeris | ||
| 48 | 00821925044944 | DSDPP100 | DISP SINUS DEBRIDER, REUSABLE PWR PACK | ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | 2 | Celeris | |
| 49 | 00821925044906 | DSD2000BA | DISP SINUS DEBRIDER, 2MM STRT, BIP, TYPE A | ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | Celeris | ||
| 50 | 00821925044890 | DSD4000BA | DISP SINUS DEBRIDER, 4MM STRT, BIP, TYPE A | ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | 2 | Celeris |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 04260293133199 | GS-950 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 2 | 04260293133175 | GS-610 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 3 | 04260293133144 | GS-325 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 4 | 04260293133106 | GS-210 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 5 | 04260293133083 | GS-060 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 6 | 04260293133076 | GS-030 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 7 | 04260293133069 | GS-015 | The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 10 The GELITA-SPON® Absorbable Gelatin Sponge, U.S.P. (“Gelita-Spon”) is made of 100% purified porcine gelatine and is of neutralcharacter in nature. GELITA-SPON® Absorbable Gelatin Sponge is non-pyrogenic. It is intended for use to control minimal bleeding bytamponade effect, blood absorption and platelet aggregation following ENT surgery. It is insoluble in water and fully absorbable.Its porous structure and interstices enables the product to absorb more than 35 times its own weight of blood and fluids. The absorptivecapacity of GELITA-SPON® is a function of its physical size, increasing as the amount of gelatine increases. It is supplied in several sizes.It is packaged individually in (double) blister, pouch or jar/container packaging, sterilized by gamma rays, and is for single use only. | GELITA-SPON® STANDARD | GELITA MEDICAL GMBH | |
| 8 | EBES603150 | 60-315 | 60-315 | Size: 1.5 x 51 x 76 mm; Type: Silicone | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 9 | EBES603140 | 60-314 | 60-314 | Size: 1.0 x 51 x 76 mm; Type: Silicone | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 10 | EBES603130 | 60-313 | 60-313 | Size: 0.50 x 51 x 76 mm; Type: Silicone | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 11 | EBES603120 | 60-312 | 60-312 | Size: 0.13 x 51 x 76 mm; Type: Silicone | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 12 | EBES603110 | 60-311 | 60-311 | Size: 0.50 x 51 x 76 mm; Type: FEP | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 13 | EBES603100 | 60-310 | 60-310 | Size: 0.25 x 51 x 76 mm; Type: FEP | Custom Nasal Splint | BOSTON MEDICAL PRODUCTS, INC. |
| 14 | EBES603040 | 60-304 | 60-304 | Size: 0.50 x 38 x 60 mm | Bivalve Nasal Splint, Large | BOSTON MEDICAL PRODUCTS, INC. |
| 15 | EBES603030 | 60-303 | 60-303 | Size: 0.25 x 38 x 60 mm | Bivalve Nasal Splint, Large | BOSTON MEDICAL PRODUCTS, INC. |
| 16 | EBES603020 | 60-302 | 60-302 | Size: 0.50 x 27 x 42 mm | Bivalve Nasal Splint, Standard | BOSTON MEDICAL PRODUCTS, INC. |
| 17 | EBES603010 | 60-301 | 60-301 | Size: 0.25 x 27 x 42 mm | Bivalve Nasal Splint, Standard | BOSTON MEDICAL PRODUCTS, INC. |
| 18 | EBES60204L0 | 60-204L | 60-204L | Type: Extra-Soft | Intranasl Splint INS | BOSTON MEDICAL PRODUCTS, INC. |
| 19 | EBES602040 | 60-204 | 60-204 | Type: Soft | Intranasl Splint INS | BOSTON MEDICAL PRODUCTS, INC. |
| 20 | EBES602030 | 60-203 | 60-203 | Doyle Open-Lumen Splint | BOSTON MEDICAL PRODUCTS, INC. | |
| 21 | EBES602020 | 60-202 | 60-202 | Doyle Combo Splint | BOSTON MEDICAL PRODUCTS, INC. | |
| 22 | EBES602010 | 60-201 | 60-201 | Nasal Airway Splint | BOSTON MEDICAL PRODUCTS, INC. | |
| 23 | 00860003136416 | SP005 | SP005 | SPIWay Endonasal Access Guide Size Medium | SPIWay | SPIWAY LLC |
| 24 | 00860003136409 | SP004 | SP004 | SPIWay Endonasal Access Guide Size Large | SPIWay | SPIWAY LLC |
| 25 | 00860003109915 | Standard | AbsorbaleGelatin Sponge | ORCA Foam | ORCA PRODUCTS, LLC | |
| 26 | 00858439001903 | 9210615 | PosiSep X2 devices are patient-comfortable sponges manufactured from naturally o PosiSep X2 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X2 devices expand when hydrated providing separation between the sinus tissues. | PosiSep X2 0.8" x 2.3" | HEMOSTASIS, LLC | |
| 27 | 00858439001880 | 9210614 | PosiSep X2 devices are patient-comfortable sponges manufactured from naturally o PosiSep X2 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X2 devices expand when hydrated providing separation between the sinus tissues. | PosiSep X2 0.7" x 1.7" | HEMOSTASIS, LLC | |
| 28 | 00858439001675 | 9210854 | PosiSep C 0.6 x 2.0 devices are patient-comfortable sponges manufactured from na PosiSep C 0.6 x 2.0 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C 0.6 x 2.0 devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | PosiSep C 0.6 x 2.0 | HEMOSTASIS, LLC | |
| 29 | 00858439001637 | 9110534 | NexPak X Intranasal Splint is a sterile flexible foam pad comprised of a lyophil NexPak X Intranasal Splint is a sterile flexible foam pad comprised of a lyophilized mixture of starch polysaccharide and polysaccharide binders. NexPak X Intranasal Splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and nasal cavity. The intranasal splint is placed in the nasal cavity after surgery or trauma. | NexPak X | HEMOSTASIS, LLC | |
| 30 | 00858439001613 | 9110524 | NexPak Intranasal Splint is a sterile flexible foam pad comprised of a lyophiliz NexPak Intranasal Splint is a sterile flexible foam pad comprised of a lyophilized mixture of starch polysaccharide and polysaccharide binders. NexPak Intranasal Splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and nasal cavity. The intranasal splint is placed in the nasal cavity after surgery or trauma. | NexPak | HEMOSTASIS, LLC | |
| 31 | 00858439001415 | 9210764 | PosiSep C² devices are patient-comfortable sponges manufactured from naturally o PosiSep C² devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C² devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | PosiSep C² | HEMOSTASIS, LLC | |
| 32 | 00858439001385 | 9210754 | PosiSep C devices are patient-comfortable sponges manufactured from naturally oc PosiSep C devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | PosiSep C | HEMOSTASIS, LLC | |
| 33 | 00858439001361 | 9210604 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | PosiSep X 8.0 cm x 1.8 cm Hemostatic Dressing/Intranasal Splint | HEMOSTASIS, LLC | |
| 34 | 00858439001330 | 9210584 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | PosiSep X 0.6 x 2.0 Hemostatic Dressing/Intranasal Splint | HEMOSTASIS, LLC | |
| 35 | 00858439001309 | 9210574 | PosiSep devices are patient-comfortable sponges manufactured from naturally occu PosiSep devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep devices expand when hydrated providing separation between the sinus tissues. | PosiSep 0.6 x 2.0 Hemostatic Dressing/Intranasal Splint | HEMOSTASIS, LLC | |
| 36 | 00858439001279 | 9210564 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | PosiSep X 0.5 x 1.5 Hemostatic Dressing/Intranasal Splint | HEMOSTASIS, LLC | |
| 37 | 00858439001248 | 9210554 | PosiSep devices are patient-comfortable sponges manufactured from naturally occu PosiSep devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep devices expand when hydrated providing separation between the sinus tissues. | PosiSep 0.5 x 1.5 Hemostatic Dressing/Intranasal Splint | HEMOSTASIS, LLC | |
| 38 | 00821925044159 | CNS155 | ChitoZolve Finished Good (8/pk) | ChitoZolve | GYRUS ACMI, INC. | |
| 39 | 00821925040557 | 70890927 | LARGE SEPTAL SPLINT UHMWPE | GYRUS ACMI, INC. | ||
| 40 | 00821925040540 | 70890926 | STANDARD SEPTAL SPLINT UHMWPE | GYRUS ACMI, INC. | ||
| 41 | 00821925040328 | 890920 | CUSTOM NASAL SPLINT, THIN SHORT - TERM USE UP TO 14 DAYS .25MM UHMWPE | GYRUS ACMI, INC. | ||
| 42 | 00821925040311 | 890919 | BIVALVE SPLINT, LARGE THICK. SHORT - TERM USE UP TO 14 DAYS .50 MM UH | GYRUS ACMI, INC. | ||
| 43 | 00821925040304 | 890918 | BIVALVE SPLINT, LARGE THIN. SHORT - TERM USE UP TO 14 DAYS .25MM UHMW | GYRUS ACMI, INC. | ||
| 44 | 00821925040298 | 890917 | BIVALVE SPLINT, STANDARD THICK. SHORT-TERM USE UP TO 14 DAYS .50 MM U | GYRUS ACMI, INC. | ||
| 45 | 00821925037755 | 890913 | SINUSPACER TURBINATE STENT | GYRUS ACMI, INC. | ||
| 46 | 00821925035119 | 140441 | NEIMAN SEPTAL SPLINT SILICONE | GYRUS ACMI, INC. | ||
| 47 | 00821925034129 | 890921 | CUSTOM NASAL SPLINT, THICK SHORT - TERM USE UP TO 14 DAYS .50MM UHMWP | GYRUS ACMI, INC. | ||
| 48 | 00821925034082 | 890916 | BIVALVE SPLINT, STANDARD THIN. SHORT-TERM USE UP TO 14 DAYS .25MM UHM | GYRUS ACMI, INC. | ||
| 49 | 00821925033658 | 890915 | NASAL SPLINT SMALL 1 - LEFT, 1 - RIGHT SILICONE SEPTAL | GYRUS ACMI, INC. | ||
| 50 | 00821925033641 | 890914 | SILICONE SEPTAL NASAL SPLINT, STANDARD 1 - LEFT, 1 - RIGHT | GYRUS ACMI, INC. |