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TMM-BCR-SOF, Tactical Medical Module- Bougie Assisted Cricothyrotomy-SOF

FDA UDI

Class II (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
TMM-BCR-SOF, Tactical Medical Module- Bougie Assisted Cricothyrotomy-SOF FDA UDI
Generic Name
Cricothyrotomy kit, single-use FDA UDI
Device Name
The TMM-BCR-SOF contains the necessary items to establish a surgical airway with a Bougie tube introducer when other methods are unsuccessful, as requested by the U.S. Millitary. FDA UDI
Model / Reference
02923 FDA UDI
Description
The TMM-BCR-SOF contains the necessary items to establish a surgical airway with a Bougie tube introducer when other methods are unsuccessful, as requested by the U.S. Millitary. FDA UDI

Identifiers

Catalog Number
02923 FDA UDI
Primary DI / UDI-DI
00856767008168 FDA UDI
FDA Product Code
OGP FDA UDI
GMDN Term
Cricothyrotomy kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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: Cricothyrotomy kit, single-use

TMM-BCR-SOF, Tactical Medical Module- Bougie Assisted Cricothyrotomy-SOF by Altitude Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cricothyrotomy kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51ed8eae-40e7-4062-906d-ef6e6bf9da5c 35 fields · synced May 30, 2026