Other products from "NATUS MEDICAL INCORPORATED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00382830056823 NT8501202 NT8501202 Pudenz Cardiac Catheter (High Pressure) JXG Shunt, Central Nervous System And Components 2 NT8501202
2 00382830001595 AuDX Pro 580-AXPRO1 The AuDX Pro Otoacoustic Emissions Measurement System is a handheld battery oper The AuDX Pro Otoacoustic Emissions Measurement System is a handheld battery operated device that performs otoacoustic emissions tests. Connection to the patient's ear is via the Bio-logic ear probe. Using a combination of hardware and software, the system produces a controlled acoustic signal in the ear canal and measures the resultiing evoked emissions that are generated by the outer hair cells of the inner ear associated with normal cochlear function. The stimuli are presented via miniature receivers and the acoustic response in the external ear canal is recorded via a miniature microphone, all embedded in the Bio-logic OAE probe. The system collects and averages data samples until specified measurement parameters are achieved. EWO Audiometer 2 AuDX Pro Otoacoustic Emissions Measurement System
3 00382830053839 Electrode Hydrogel 200249-507, 62050, 62051 Neonatal EEG Hydrogel sensor OMA,OMC Amplitude-Integrated Electroencephalograph,Reduced- Montage Standard Electroencephalograph 2 Olympic CFM
4 00382830052160 Disposable Electrodes 101605 Square Square Snap Electrodes - aggressive adhesion (not for use on infants) EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Biologic
5 00382830003971 Mattress Covers 58106 Disposable Mattress Covers, one-piece mattress for Bili-Bassinet LBI Unit, Neonatal Phototherapy Olympic Bili-Bassinet
6 00382830003964 Mattress Covers 58105 Disposable Mattress Covers, mattress with separate bolster for Olympic Bili-Bassinet LBI Unit, Neonatal Phototherapy Olympic Bili-Bassinet
7 00382830001885 011445 011445 Bio-Logic Algo Supplies kit containing Flexicouplers and JellyTabs intended to b Bio-Logic Algo Supplies kit containing Flexicouplers and JellyTabs intended to be used with Natus hearing screeners. GXY,GWJ Electrode, Cutaneous,Stimulator, Auditory, Evoked Response Bio-Logic Algo Supplies
8 00382830048859 025420 025420 Patient Monitor Cable GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
9 00382830058049 NTVTUN NTVTUN Camino Flex Ventricular Intracranial Pressure Monitoring Kit GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
10 00382830054942 Echo-Screen III The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
11 00382830053648 Gold Disc Electrode Silicone 101007 Reusable Gold Disc electrode tangle free EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
12 00382830048866 026950 026950 14.4 V Lithium Ion Battery GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
13 00382830049023 CAM02 CAM02 Intracranial Pressure and Temperature Monitor GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
14 00382830048705 025430 025430 18 V DC 1.67 A, 30 W AC Power Adapter GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
15 00382830048699 025440 025440 USB-to-RS232 Adapter Cable GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
16 00382830048675 FLEXEXT FLEXEXT Camino Flex Extension Cable GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
17 00382830048668 CAMCABL CAMCABL Fiber Optic Catheter Cable GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
18 00382830047548 110-4L 1104L CAMINO INTRCRANIAL PRESSURE MONITORING CATHETER WITH LICOX IMC BOLT FITTING GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
19 00382830047531 110-4HMT 1104HMT MICRO VENTRICULAR BOLT PRESSURE-TEMPERATURE MONITORING KIT GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
20 00382830047524 110-4HM 1104HM MICRO VENTRICULAR BOLT PRESSURE MONITORING KIT GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
21 00382830047517 110-4G 1104G POST CRANIOTOMY SUBDURAL PRESSURE MONITORING KIT GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
22 00382830047500 110-4BT 1104BT INTRACRANIAL PRESSURE-TEMPERATURE MONITORING KIT GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
23 00382830047494 110-4B 1104B OLM INTRACRANIAL PRESSURE MONITORING KIT GWM Device, Monitoring, Intracranial Pressure 2 CAMINO®
24 00382830045353 EchoScreen III Refurbished, DPOAE & ABR with barcode 023485R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
25 00382830045339 EchoScreen III Refurbished, TEOAE & ABR with barcode 023484R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
26 00382830045315 EchoScreen III Refurbished, TEOAE & DPOAE with barcode 023483R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
27 00382830045292 EchoScreen III Refurbished, ABR with barcode 023482R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
28 00382830045278 EchoScreen III Refurbished, DPOAE with barcode 023481R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
29 00382830045247 EchoScreen III Refurbished, TEOAE with barcode 023480R The Echo-Screen III hearing screener is a portable, handheld, battery-operated d The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies. EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response 2 Echo-Screen III Pro
30 00382830000901 Silver Disc ElectrodeTeflon 101001-T Reusable Silver Disc Electrode teflon lead EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
31 00382830001618 Scout Sport 580-SP2191 The Scout Sport Otoacoustix Emissions Measurement System delivers controlled aco The Scout Sport Otoacoustix Emissions Measurement System delivers controlled acoustic signals in the ear canal and measures the resulting evoked otoacoustic emissions (OAEs) that are generated by the outer hair cells of the inner ear. The Scout Sport device performs transient evoked otoacoustic emissions (TEOAE), distortion product otoacoustic emissions (DPOAE), and DPOAE input/output (I/O) tests. EWO Audiometer 2 Scout Sport Otoacoustic Emissions Measurement System
32 00382830000888 Silver-Chloride Disc Electrode Silicone 101004 Resuable Silver-Chloride Disc Electrode silicon leads EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
33 00382830001489 Silver Disc Electrode 101091 Reusable Molded Silver EEG 10mm Disc Electrodes with 48" (1.2m) PVC lead wires EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
34 00382830000918 Gold Disc Electrode Teflon 101007-T Reusable Gold Disc electrode teflon leads EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
35 00382830000871 Silver Disc Electrode Silicone 101001 Reusable Silver Disc Electrod silicone leads EWO,GWJ Audiometer,Stimulator, Auditory, Evoked Response Natus
36 00382830044059 030697 Preamplifier 3 Cable GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
37 00382830044035 010726 ALGO 3i Acoustic Transducer Assembly (ATA) Cable GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
38 00382830043960 000696 ALGO 5 Patient Cable Assembly (PCA) Cable GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
39 00382830044615 013504 Echo-Screen III Pro Hearing Screening Device TEOAE and DPOAE set GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
40 00382830044608 013513 Echo-Screen III Pro Hearing Screening Device TEOAE and DPOAE set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
41 00382830044585 013512 Echo-Screen III Pro Hearing Screening Device ABR set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
42 00382830044561 013511 Echo-Screen III Pro Hearing Screening Device DPOAE set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
43 00382830044554 013501 Echo-Screen III Pro Hearing Screening Device DPOAE set GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
44 00382830053297 Algo 3i 040695, 040969 The ALGO® 3i Newborn Hearing Screener is a portable, noninvasive device for scre The ALGO® 3i Newborn Hearing Screener is a portable, noninvasive device for screening the hearing of infants between the ages of 34 weeks corrected gestational age and six months. The screener uses Natus’ AABR® technology. Babies should be well enough for hospital discharge, and should be asleep or in a quiet state at the time of screening. The ALGO 3i screener is simple to operate and does not require special technical skills or interpretation of results. Basic training with the equipment is sufficient to learn how to screen infants correctly. A typical screening can be completed in 15 minutes or less in any clinical environment (i.e. well-baby nursery, NICU, mother’s bedside, audiology suite, outpatient clinic, or doctor’s office). GWJ Stimulator, Auditory, Evoked Response 2 ALGO 3i Newborn Hearing Screener
45 00382830044547 013510 Echo-Screen III Pro Hearing Screening Device TEOAE set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
46 00382830044738 009149 PCA Electrode Cable for Echo-Screen III Devices GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
47 00382830044721 010999 ATA Transducer for Echo-Screen III Devices GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
48 00382830044660 013516 Echo-Screen III Pro Hearing Screening Device TEOAE, DPOAE and ABR set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
49 00382830044653 013506 Echo-Screen III Pro Hearing Screening Device TEOAE, DPOAE and ABR set GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
50 00382830044646 013515 Echo-Screen III Pro Hearing Screening Device DPOAE and ABR set w/o Barcode Scanner GWJ Stimulator, Auditory, Evoked Response 2 NATUS MEDICAL
Other products with the same Product Code "GYK"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00763000260026 48405 PASSER 48405 CATH V/P SUBCUT 60CM N/A MEDTRONIC PS MEDICAL, INC.
2 00763000260019 48403 PASSER 48403 L/P SUBCUT CATH 38CM N/A MEDTRONIC PS MEDICAL, INC.
3 00763000031268 48405 PASSER 48405 CATH V/P SUBCUT 60CM N/A MEDTRONIC PS MEDICAL, INC.
4 00382830058179 NT9MD1241 NT9MD1241 PERITONEAL INTRODUCER SHEATHS, 81 cm Natus® NATUS MEDICAL INCORPORATED
5 00382830057332 NT8502002 NT8502002 Disposable Peritoneal Catheter Passer (36 cm) Natus® NATUS MEDICAL INCORPORATED
6 00382830057325 NT8502001 NT8502001 Disposable Peritoneal Catheter Passer (60 cm) Natus® NATUS MEDICAL INCORPORATED
7 00382830055208 NT990012 NT990012 PERITONEAL INTRODUCER SHEATHS, 31 cm Natus® NATUS MEDICAL INCORPORATED
8 00382830054140 NT9MD170 NT9MD170 PERITONEAL INTRODUCER SHEATH, 70 cm (27.5 Inches) Natus® NATUS MEDICAL INCORPORATED
9 00382830054119 NT901118 NT901118 PERITONEAL INTRODUCER SHEATHS, 46 cm Natus® NATUS MEDICAL INCORPORATED
10 00382830053624 NT901124 NT901124 PERITONEAL INTRODUCER SHEATHS, 61 cm Natus® NATUS MEDICAL INCORPORATED
11 20886704042744 83-1326 831326 CODMAN Peel-Away Catheter Introducer 14 FR. CODMAN CODMAN & SHURTLEFF, INC.
12 20886704042737 83-1325 831325 CODMAN Peel-Away Catheter Introducer 12.5 FR. CODMAN CODMAN & SHURTLEFF, INC.
13 20886704042720 83-1323 831323 CODMAN Peel-Away Catheter Introducer 9 Fr. CODMAN CODMAN & SHURTLEFF, INC.
14 10885403070501 NL850-2070 NL850-2070 V. Mueller LUMBAR PERITONEAL SUBCUTANEOUS CATHETER PASSER V. Mueller CAREFUSION 2200, INC
15 10885403070495 NL850-2050 NL850-2050 V. Mueller PERITONEAL SHUNT PASSER NON-STERILE V. Mueller CAREFUSION 2200, INC
16 10885403070488 NL850-2010 NL850-2010 V. Mueller SUBCUT ANEOUS PERITONEAL CATHETER PASSER V. Mueller CAREFUSION 2200, INC
17 10885403070464 NL850-2000 NL850-2000 V. Mueller PORTNOY PERITONEAL TROCAR OVERALL LENGTH 38 CM V. Mueller CAREFUSION 2200, INC
18 10866614000198 41.240.503 41.240.503 The Subcutaneous Guidewire is designed to facilitate the subcutaneous passage of The Subcutaneous Guidewire is designed to facilitate the subcutaneous passage of tubing, suture, ribbons, and/or bands between two skin incisions. It is also designed to facilitate the subcutaneous passage of shunt tubing when implanting a ventricular or lumbar cerebrospinal fluid (CSF) shunting system or externalized CSF drain. Subcutaneous Guidewire - Large ARKIS BIOSCIENCES INC.
19 10866614000181 41.240.502 41.240.502 The Subcutaneous Guidewire is designed to facilitate the subcutaneous passage of The Subcutaneous Guidewire is designed to facilitate the subcutaneous passage of tubing, suture, ribbons, and/or bands between two skin incisions. It is also designed to facilitate the subcutaneous passage of shunt tubing when implanting a ventricular or lumbar cerebrospinal fluid (CSF) shunting system or externalized CSF drain. Subcutaneous Guidewire - Medium ARKIS BIOSCIENCES INC.
20 10381780521419 831326 83-1326 Peel-Away Catheter Introducer CODMAN® INTEGRA LIFESCIENCES PRODUCTION CORPORATION
21 10381780521402 831325 83-1325 Peel-Away Catheter Introducer CODMAN® INTEGRA LIFESCIENCES PRODUCTION CORPORATION
22 10381780521396 831323 83-1323 Peel-Away Catheter Introducer CODMAN® INTEGRA LIFESCIENCES PRODUCTION CORPORATION
23 10381780072379 NL8502002 NL8502002 36CM DISP PASSER PKG ASSYThe Disposable Subcutaneous Peritoneal Catheter Passer 36CM DISP PASSER PKG ASSYThe Disposable Subcutaneous Peritoneal Catheter Passer is a two-component instrument consisting of a stainless tubular shaft with an ULTEM obturator. This product is used to provide a subcutaneous tunnel between the flushing-device site and the incision for the peritoneal catheter. The catheter consists of an open tubular shaft, concentric with a T-handled obturator which extends beyond the tubular shaft. The instrument is passed subcutaneously with the obturator assembled in the tubular shaft. Once the obturator has been removed, the catheter tubing can be passed and the tubular shaft portion of the instrument can be removed in either direction. Integra Disposable Peritoneal Catheter Passer INTEGRA LIFESCIENCES CORPORATION
24 10381780072362 NL8502001 NL8502001 60CM DISP PASSER PKG ASSYThe Disposable Subcutaneous Peritoneal Catheter Passer 60CM DISP PASSER PKG ASSYThe Disposable Subcutaneous Peritoneal Catheter Passer is a two-component instrument consisting of a stainless tubular shaft with an ULTEM obturator. This product is used to provide a subcutaneous tunnel between the flushing-device site and the incision for the peritoneal catheter. The catheter consists of an open tubular shaft, concentric with a T-handled obturator which extends beyond the tubular shaft. The instrument is passed subcutaneously with the obturator assembled in the tubular shaft. Once the obturator has been removed, the catheter tubing can be passed and the tubular shaft portion of the instrument can be removed in either direction. Integra Disposable Peritoneal Catheter Passer INTEGRA LIFESCIENCES CORPORATION
25 10381780034421 990012 The 31 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal The 31 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal Introducer of appropriate length (31 cm) during the placement of a peritoneal drainage catheter in the treatment of hydrocephalus. It features a tapered tip to facilitate subcutaneous insertion and passage. Integra® INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
26 10381780034414 990010 The Tunneler is a single-use instrument consisting of a stainless steel cannula The Tunneler is a single-use instrument consisting of a stainless steel cannula with removable handle, plastic line with bullet-shaped end and barbed end, and sheath. The tunneler (65 cm) is used to make a subcutaneous tunnel between two incisions for procedures such as the subcutaneous insertion of the peritoneal drainage catheter of a hydrocephalus shunt. The barbed end is intended to be connected to a 0.8 to 1.4 mm internal diameter catheter. Integra® INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
27 10381780034391 990001 The Tunneler is a single-use instrument consisting of a stainless steel cannula The Tunneler is a single-use instrument consisting of a stainless steel cannula with removable handle, plastic line with bullet-shaped end and barbed end, and sheath. The tunneler (45 cm) is used to make a subcutaneous tunnel between two incisions for procedures such as the subcutaneous insertion of the peritoneal drainage catheter of a hydrocephalus shunt. The barbed end is intended to be connected to a 0.8 to 1.4 mm internal diameter catheter. Integra® INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
28 10381780033202 901124 The 61 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal The 61 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal Introducer of appropriate length (61 cm) during the placement of a peritoneal drainage catheter in the treatment of hydrocephalus. It features a tapered tip to facilitate subcutaneous insertion and passage. Integra® INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
29 10381780033172 901118 The 46 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal The 46 cm Peritoneal Introducer Sheath is designed to be used with a Peritoneal Introducer of appropriate length (46 cm) during the placement of a peritoneal drainage catheter in the treatment of hydrocephalus. It features a tapered tip to facilitate subcutaneous insertion and passage. Integra® INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
30 03760124134810 SP04 Disposable catheter passer with sheath, 65 cm length Phoenix Neuro SOPHYSA
31 03760124134803 SP03 Disposable catheter passer with sheath, 45 cm length Phoenix Neuro SOPHYSA
32 03760124133813 SP05 Disposable catheter passer with sheath, 30 cm length Phoenix Neuro SOPHYSA
33 00866614000177 41.020.503 41.020.503 The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin. Precision Tunneler - Large ARKIS BIOSCIENCES INC.
34 00866614000160 41.020.502 41.020.502 The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin. Precision Tunneler - Medium ARKIS BIOSCIENCES INC.
35 00866614000153 41.020.501 41.020.501 The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin. Precision Tunneler - Small ARKIS BIOSCIENCES INC.
36 00866614000146 41.157.101 41.157.101 The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneo The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin. Single Pass Tunneling Guidewire - Small ARKIS BIOSCIENCES INC.
37 00866614000139 41.157.102 41.157.102 The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneo The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin. Single Pass Tunneling Guidewire - Medium ARKIS BIOSCIENCES INC.
38 00866614000122 41.157.103 41.157.103 The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneo The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin. Single Pass Tunneling Guidewire - Large ARKIS BIOSCIENCES INC.