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7ft O2 Delivery Tube TAV, 1PK

FDA UDI

Class II (US FDA UDI)

by Inogen, Inc.

Identity

Trade Name
7ft O2 Delivery Tube TAV, 1PK FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
7ft O2 Delivery Tube TAV, 1PK, RP-1010 FDA UDI
Model / Reference
RP-1010 FDA UDI
Description
7ft O2 Delivery Tube TAV, 1PK, RP-1010 FDA UDI

Identifiers

Catalog Number
RP-1010 FDA UDI
Primary DI / UDI-DI
00817131020384 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

No

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

7ft O2 Delivery Tube TAV, 1PK 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 df432ece-52ef-48c3-ab7e-1e7608a4c4a1 36 fields · synced May 30, 2026