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Medical Operator Kit, (TMK-MO), Black w/SOFTT-W

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Medical Operator Kit, (TMK-MO), Black w/SOFTT-W FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Specifically designed with input from the Special Operations community to meet the demand for a low-profile medical backpack. FDA UDI
Model / Reference
01326BK FDA UDI
Description
Specifically designed with input from the Special Operations community to meet the demand for a low-profile medical backpack. FDA UDI

Identifiers

Catalog Number
01326BK FDA UDI
Primary DI / UDI-DI
00850018892100 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
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: First aid kit, non-medicated, single-use

Medical Operator Kit, (TMK-MO), Black w/SOFTT-W by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f129aeb-7188-4099-99f1-52dead04c3e3 35 fields · synced May 30, 2026