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TMM-NPA Naso Airway Module

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
TMM-NPA Naso Airway Module FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
Nasopharyngeal Airway module with sizes from 20fr to 36fr. Each airway individually packaged with lubricant. FDA UDI
Model / Reference
02118 FDA UDI
Description
Nasopharyngeal Airway module with sizes from 20fr to 36fr. Each airway individually packaged with lubricant. FDA UDI

Identifiers

Primary DI / UDI-DI
00856767008007 FDA UDI
FDA Product Code
BTQ FDA UDI
GMDN Term
First aid kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5100 FDA UDI
Commercial Distribution
Not 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

Yes

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

TMM-NPA Naso Airway Module by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87e7f0bd-32de-4fde-8f91-1a059d0aaf80 34 fields · synced May 30, 2026