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Cpr Or Sprains Treatment Pack

FDA UDI

Class I (US FDA UDI)

by Uline, Inc.

Identity

Trade Name
CPR OR SPRAINS TREATMENT PACK FDA UDI
Generic Name
First aid kit, non-medicated, reusable FDA UDI
Device Name
4.25" X 24" FLEX PADDED SPLINT ARC FIRST AID GUIDE ANSI 2021 NITRILE EXAM GLOVES 2/BAG ANSI TRIANGULAR BDG 1/BAG COLD PACK 4X5 BULK CPR FACE SHIELD W/1-WAY VALVE FDA UDI
Model / Reference
S-25617 FDA UDI
Description
4.25" X 24" FLEX PADDED SPLINT ARC FIRST AID GUIDE ANSI 2021 NITRILE EXAM GLOVES 2/BAG ANSI TRIANGULAR BDG 1/BAG COLD PACK 4X5 BULK CPR FACE SHIELD W/1-WAY VALVE FDA UDI

Identifiers

Primary DI / UDI-DI
10850015055604 FDA UDI
FDA Product Code
OHO FDA UDI
GMDN Term
First aid kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, non-medicated, reusable

Cpr Or Sprains Treatment Pack by Uline, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uline, Inc.

Sources (1)

  • FDA UDI 908e40ed-95e4-4605-ac3f-b5f9d1ab4bbf 33 fields · synced Jun 8, 2026