← Back to catalogue

TMM-DE (Tactical Medical Module-Dental)

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
TMM-DE (Tactical Medical Module-Dental) FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, medicated, single-use FDA UDI
Device Name
General purpose Dental Tray-Kit FDA UDI
Model / Reference
01350 FDA UDI
Description
General purpose Dental Tray-Kit FDA UDI

Identifiers

Catalog Number
01350 FDA UDI
Primary DI / UDI-DI
00850013417087 FDA UDI
FDA Product Code
OFX FDA UDI
GMDN Term
Dental/maxillofacial surgical procedure kit, medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

Yes

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: Dental/maxillofacial surgical procedure kit, medicated, single-use

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

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Altitude Technologies Inc.

Sources (1)

  • FDA UDI 929f4153-4a85-463e-9246-346b853242a7 35 fields · synced Jun 8, 2026