Forward Medical Emergency First Aid Kit Plus (ME-FAK Plus)

FDA UDI

Class I (US FDA UDI)

by Integrated Medcraft Llc

Identity

Trade Name: Forward Medical Emergency First Aid Kit Plus (ME-FAK Plus) FDA UDI
Generic Name: First aid kit, non-medicated, single-use FDA UDI
Device Name: First aid box that contains the following items; Tourniquet, Trauma Dressing, Compressed Gauze, Quik Clot Bleeding Control Dressing, Chest Seal, Emergency Blanket, Tape, Shears and gloves. FDA UDI
Model / Reference: 1011-10010 FDA UDI
Description: First aid box that contains the following items; Tourniquet, Trauma Dressing, Compressed Gauze, Quik Clot Bleeding Control Dressing, Chest Seal, Emergency Blanket, Tape, Shears and gloves. FDA UDI

Identifiers

Primary DI / UDI-DI: 00850056748100 FDA UDI
FDA Product Code: OHO FDA UDI
GMDN Term: First aid kit, non-medicated, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid kit, non-medicated, single-use

Forward Medical Emergency First Aid Kit Plus (ME-FAK Plus) by Integrated Medcraft Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, single-use.

IFAK — FARETEC, INC. · Class I
NAR Kit — NORTH AMERICAN RESCUE, LLC.
NAR Kit — NORTH AMERICAN RESCUE, LLC.
NAR Kit — NORTH AMERICAN RESCUE, LLC.
NAR Kit — NORTH AMERICAN RESCUE, LLC.
NAR — NORTH AMERICAN RESCUE, LLC.
NAR Kit — NORTH AMERICAN RESCUE, LLC.
NAR — NORTH AMERICAN RESCUE, LLC. · Class I

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 I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Integrated Medcraft Llc

Sources (1)

FDA UDI 7bbabf49-611e-4677-834d-aec8a54bad88 33 fields · synced Jun 8, 2026