Emergency Medical Products

FDA UDI

Class II (US FDA UDI)

by Emergency Medical Products, Inc.

Identity

Trade Name: Emergency Medical Products FDA UDI
Generic Name: First aid kit, medicated FDA UDI
Device Name: Contents for Latex-free 1st Call-in Bag FDA UDI
Model / Reference: FCB-CLF FDA UDI
Description: Contents for Latex-free 1st Call-in Bag FDA UDI

Identifiers

Primary DI / UDI-DI: 00851772007090 FDA UDI
FDA Product Code: CBP FDA UDI
DXQ FDA UDI
CAN FDA UDI
GMDN Term: First aid kit, medicated FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5870 FDA UDI
870.1120 FDA UDI
868.2700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: First aid kit, medicated

Emergency Medical Products by Emergency Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as First aid kit, medicated.

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OP - First aid series — Yiwu Ori-Power Medtech Co., Ltd. · N
HSB - National Standard Body Fluid — Certified Safety Manufacturing, Inc. · N
First Aid Only — Acme United Corporation · N
First Aid Only — ACME UNITED CORP. · N
NAR — NORTH AMERICAN RESCUE, LLC.
OP - First aid series — Yiwu Ori-Power Medtech Co., Ltd. · N

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Emergency Medical Products, Inc.

Sources (1)

FDA UDI 7b9f48ac-23ea-4faa-af82-256a6054d479 33 fields · synced May 29, 2026