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Mass Casualty Critical Intervention Kit, (LEMK-MCCI), Refill w/CAT, Contents On…

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Mass Casualty Critical Intervention Kit,(LEMK-MCCI), Refill w/CAT, Contents Only FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Law Enforcement Medical Kit - Mass Casualty Critical Intervention Kit (LEMK-MCCI). FDA UDI
Model / Reference
01155REF-CAT FDA UDI
Description
Law Enforcement Medical Kit - Mass Casualty Critical Intervention Kit (LEMK-MCCI). FDA UDI

Identifiers

Catalog Number
01155REF-CAT FDA UDI
Primary DI / UDI-DI
00850013417742 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Mass Casualty Critical Intervention Kit, (LEMK-MCCI), Refill w/CAT, Contents On… by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05473f18-9f86-43f4-8736-e01a993a2510 35 fields · synced Jun 1, 2026