Duns Number:039612668
Device Description: (4) ABSORBENT COMPRESS,(25) ANTACID,(50) ANTIBIOTIC OINTMENT,(54) ANTISEPTIC TOWELETTE,(25 (4) ABSORBENT COMPRESS,(25) ANTACID,(50) ANTIBIOTIC OINTMENT,(54) ANTISEPTIC TOWELETTE,(25) ASPIRIN,(2) BURN DRESSING,(1) COHESIVE ELASTIC BANDAGE,(100) COTTON SWAB,(75) COUGH DROPS,(2) CPROTECTOR,(25) EXTRA-STRENGTH ACETAMINOPHEN,(16) EYE PAD WITH TAPE,(25) FABRIC FINGERTIP BANDAGE,(25) FABRIC KNUCKLE BANDAGE,(50) BURN CREAM,(1) FIRST AID FACTS GUIDE,(3) FIRST AID TAPE,(25) GAUZE PAD,(4) 2" X 6 YD GAUZE ROLL,(2) 4" X 6 YD GAUZE ROLL,(23) HAND SANITIZER,(25) IBUPROFEN,(2) INSTANT ICE PACK,(4) NITRILE GLOVE 1,(25) NON-STICK PAD,(100) PLASTIC BANDAGE,(1) PLASTIC TWEEZERS,(1) SAM SPLINT,(1) SCISSORS,(1) SINGLE USE SALINE,(10) STING WIPES,(1) TOURNIQUET,(1) TRAUMA DRESSING,(3) TRIANGULAR BANDAGE,(1) TOPICAL POWDER,(50) 3/4" X 3" PLASTIC BANDAGE,(25) 2" X 3" PLASTIC BANDAGE,(50) FABRIC BANDAGE,(1) EMERGENCY RESCUE BLANKET,(1) ABSORBENT POWDER,(1) BAG WITH SCOOP,(1) BIOHAZARD BAG,(1) DISPOSABLE FACE MASK WITH SHIELD,(2) GERMICIDAL WIPE,(1) INFECTION CONTROL GOWN,(2) NITRILE GLOVE 2,(2) PAPER TOWEL,(1) PLEATED BOUFFANT
Catalog Number
-
Brand Name
ANSI First Aid Kit Class B+, 250 Person
Version/Model Number
H-9997
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
Yes
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
CBP
Product Code Name
Valve, Non-Rebreathing
Public Device Record Key
3d19f601-aa2a-48a7-a5f3-c6625768b114
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
March 22, 2022
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 8 |
2 | A medical device with a moderate to high risk that requires special controls. | 1 |
U | Unclassified | 2 |