← Back to catalogue

McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Non-fixed medical gas cylinder regulator FDA UDI
Device Name
Oxygen Regulator MINI CGA870 CONNECTION | BARB OUTLET | T-HANDLE | GREEN 0-15 LPM (20/cs) FDA UDI
Model / Reference
146-18302GMN FDA UDI
Description
Oxygen Regulator MINI CGA870 CONNECTION | BARB OUTLET | T-HANDLE | GREEN 0-15 LPM (20/cs) FDA UDI

Identifiers

Primary DI / UDI-DI
00612479262041 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Non-fixed medical gas cylinder 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-fixed medical gas cylinder regulator

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-fixed medical gas cylinder regulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI b7ffab5c-e569-44a2-ba9c-70aeaa388358 33 fields · synced May 30, 2026