Duns Number:176528040
Device Description: 1151 -1.000 EACH GG 3 Shelf Cabinet Emp w/Pkt6300 -1.000 EACH GG 7/8x3 Fabric Strip Bandag 1151 -1.000 EACH GG 3 Shelf Cabinet Emp w/Pkt6300 -1.000 EACH GG 7/8x3 Fabric Strip Bandage (50)6302 -1.000 EACH GG Fingertip Bandage (40) +6304 -1.000 EACH GG Knuckle Bandage (40) +6254- 1.000 EACH Waterproof Tape 1"x5 yds6206 -1.000 EACH GG 3x3 Gauze Pads (25)6102 -1.000 EACH 2" RIP-N-WRAP6400 -2.000 EACH GG Triangular Bandage +2206 - 1.000 EACH Sinus relief (100)2280 -1.000 EACH GG Max Str Stomach relief 100ct3302 -2.000 EACH GG Cold Pack Medium/Boxed +4105 -1.000 EACH GG 4oz Eye Wash4106 -1.000 EACH GG 8oz Eye Wash2224 -1.000 EACH Maximum Non-Aspirin (100)80548 - 1.000 EACH MF Aspirin 250s6213 -4.000 EACH 5x9 Combine Dressing ABD3005 -1.000 U GG Cold Spray 4 oz3004 -1.000 EACH GG Hydrogen Peroxide 2oz pump1150PI -D 1.000 EACH Pocket Items 3 Shelf Kit6314 -1.000 EACH GG 1x3 Plastic Strip Bandage (60)66002 -1.000 EACH Latex Free Tourniquet76001- 1.000 EACH Multi-Purpose Splint Folded6112 -2.000 EACH 2" Stretch Roller Gauze NS6114 -1.000 EACH 4" Stretch Roller Gauze3106 -1.000 EACH GG Derma-Caine Burn Cream (25)3101 -1.000 EACH GG Tri-Antibiotic Ointment (25)3025 2-.000 U GG Antiseptic Towelettes (25)80201 -1.000 EACH CPR Mask3160 2-.000 EACH WJ Burn Dressing 4x46252 -1.000 EACH Tape 1/2" X 2 1/2 YANSI-B -1.000 EACH ANSI STICKER B
Catalog Number
1150
Brand Name
Grenn Guard Three-Shelf First Aid Cabinet
Version/Model Number
1150
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LRR
Product Code Name
First Aid Kit With Drug
Public Device Record Key
50301f26-d8ac-4b62-8b2a-94bce25c649a
Public Version Date
July 23, 2019
Public Version Number
1
DI Record Publish Date
July 15, 2019
Package DI Number
50347682011500
Quantity per Package
1
Contains DI Package
00347682011505
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
master case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 36 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1 |
| U | Unclassified | 1 |