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Tactical Medical Module-Chest Wound (TMM-CW)

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Tactical Medical Module-Chest Wound (TMM-CW) FDA UDI
Generic Name
Body aspiration needle, single-use FDA UDI
Device Name
The Chinook Tactical Medical Module - Chest Wound (TMM-CW) contains just those essential items for the treatment of chest decompression and sucking chest wound injuries. FDA UDI
Model / Reference
01353 FDA UDI
Description
The Chinook Tactical Medical Module - Chest Wound (TMM-CW) contains just those essential items for the treatment of chest decompression and sucking chest wound injuries. FDA UDI

Identifiers

Catalog Number
01353 FDA UDI
Primary DI / UDI-DI
00850018201384 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Body aspiration needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Body aspiration needle, single-use

Tactical Medical Module-Chest Wound (TMM-CW) by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body aspiration needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3900ea0-a20f-4b15-b436-5d36de8e1ecf 35 fields · synced May 31, 2026