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TAV 50ft O2 Delivery Tubing

FDA UDI

Class II (US FDA UDI)

by Inogen, Inc.

Identity

Trade Name
TAV 50ft O2 Delivery Tubing FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
TAV 50ft O2 Delivery Tubing, 10-09891-XX-01 FDA UDI
Model / Reference
10-09891-XX-01 FDA UDI
Description
TAV 50ft O2 Delivery Tubing, 10-09891-XX-01 FDA UDI

Identifiers

Primary DI / UDI-DI
00817131020247 FDA UDI
510(k) Number
K152664 FDA UDI
FDA Product Code
ONZ FDA UDI
GMDN Term
Oxygen administration tubing 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

No

FDA UDI

Category: Oxygen administration tubing

TAV 50ft O2 Delivery Tubing by Inogen, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen administration tubing.

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 63b1f72d-0172-43ca-8c72-7a2f3d97cd17 35 fields · synced May 30, 2026