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Wellead OXYGEN TUBING

FDA UDI

Class I (US FDA UDI)

by Well Lead Medical Co., Ltd

Identity

Trade Name
Wellead OXYGEN TUBING FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
10ft(3.05m)NON STERILE FDA UDI
Model / Reference
R01C01301F FDA UDI
Description
10ft(3.05m)NON STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
06936881166778 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

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: Oxygen administration tubing

Wellead OXYGEN TUBING by Well Lead Medical Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen administration tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a0354d78-e26b-4278-aca5-65d2c65755e5 33 fields · synced May 30, 2026