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TMK-UTQ Pouch, OD

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
TMK-UTQ Pouch, OD FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
The Tactical Medical Kit-Universal Turniquet (TMK-UTQ) pouch is designed to fit most tourniquets on the market. FDA UDI
Model / Reference
601324OD FDA UDI
Description
The Tactical Medical Kit-Universal Turniquet (TMK-UTQ) pouch is designed to fit most tourniquets on the market. FDA UDI

Identifiers

Catalog Number
601324OD FDA UDI
Primary DI / UDI-DI
00850018201780 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
Not 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

TMK-UTQ Pouch, OD by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef2f75dd-473d-4d3e-99a2-01d180fae877 36 fields · synced Jun 1, 2026