ANSI First Aid Kit Class B+, 250 Person - (4) ABSORBENT COMPRESS,(25) ANTACID,(50) - ULINE, INC.

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

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More Product Details

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

Product Characteristics

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 Details

Product Code

CBP

Product Code Name

Valve, Non-Rebreathing

Device Record Status

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

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ULINE, INC." Characteristics
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