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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 therapy conserving regulator FDA UDI
Device Name
REGULATOR 0-8 W/GAUGE YOKE STY FDA UDI
Model / Reference
JB0150-081 FDA UDI
Description
REGULATOR 0-8 W/GAUGE YOKE STY FDA UDI

Identifiers

Catalog Number
JB0150-081 FDA UDI
Primary DI / UDI-DI
M368JB01500811 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Oxygen therapy conserving regulator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2700 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

No

FDA UDI

Over-the-Counter

Yes

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 therapy conserving regulator

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 therapy conserving regulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cc842af-64e9-41a7-bb47-6455a35b8a6a 35 fields · synced Jun 1, 2026