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Hypothermia Management Kit, (TMM-HMK)

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Hypothermia Management Kit, (TMM-HMK) FDA UDI
Generic Name
Hypothermia-prevention whole-body suit FDA UDI
Device Name
The Tactical Medical Module Hypothermia Management Kit provides prevention and management of hypothermia. FDA UDI
Model / Reference
01361 FDA UDI
Description
The Tactical Medical Module Hypothermia Management Kit provides prevention and management of hypothermia. FDA UDI

Identifiers

Catalog Number
01361 FDA UDI
Primary DI / UDI-DI
00850018201391 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Hypothermia-prevention whole-body suit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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: Hypothermia-prevention whole-body suit

Hypothermia Management Kit, (TMM-HMK) by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypothermia-prevention whole-body suit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ec064090-de19-4cd5-aa4b-559d85e5449b 35 fields · synced May 30, 2026