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TMM-CT (Tactical Medical Module-Chest Tube)

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
TMM-CT (Tactical Medical Module-Chest Tube) FDA UDI
Generic Name
Pneumothorax catheter insertion set FDA UDI
Device Name
Catheter, Irrigation FDA UDI
Model / Reference
01378 FDA UDI
Description
Catheter, Irrigation FDA UDI

Identifiers

Catalog Number
01378 FDA UDI
Primary DI / UDI-DI
00850013417063 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Pneumothorax catheter insertion set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Pneumothorax catheter insertion set

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

Similar devices

Also classified as Pneumothorax catheter insertion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Altitude Technologies Inc.

Sources (1)

  • FDA UDI 5ae497c8-a466-4915-9939-eebc98899d14 35 fields · synced Jun 6, 2026