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TAV Nasal Interface

FDA UDI

Class II (US FDA UDI)

by Inogen, Inc.

Identity

Trade Name
TAV Nasal Interface FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
TAV Nasal Interface (10-09815-XX-01) FDA UDI
Model / Reference
10-09815-XX-01 FDA UDI
Description
TAV Nasal Interface (10-09815-XX-01) FDA UDI

Identifiers

Primary DI / UDI-DI
00817131020308 FDA UDI
510(k) Number
K152664 FDA UDI
FDA Product Code
ONZ FDA UDI
GMDN Term
CPAP/BPAP nasal mask, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: CPAP/BPAP nasal mask, reusable

TAV Nasal Interface by Inogen, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP nasal mask, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inogen, Inc.

Sources (1)

  • FDA UDI dec10e2e-5b86-4a77-8fe8-07785da98970 35 fields · synced May 30, 2026