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John Bunn

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
John Bunn FDA UDI
Generic Name
Oxygen administration kit FDA UDI
Device Name
MASK 02W/7ft TUBING ADLT 50/CS FDA UDI
Model / Reference
GF64041 FDA UDI
Description
MASK 02W/7ft TUBING ADLT 50/CS FDA UDI

Identifiers

Catalog Number
GF64041 FDA UDI
Primary DI / UDI-DI
M368GF640411 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Oxygen administration kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 FDA UDI
Commercial Distribution
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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oxygen administration kit

John Bunn by GF Health Products, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen administration kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c50a989a-31f1-4079-8107-a7d8c7210829 35 fields · synced May 30, 2026