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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
Oxygen Regulator STANDARD CGA870 CONNECTION | BARB OUTLET | T-HANDLE | GREEN 0-15 LPM (20/cs) FDA UDI
Model / Reference
146-18302GN FDA UDI
Description
Oxygen Regulator STANDARD CGA870 CONNECTION | BARB OUTLET | T-HANDLE | GREEN 0-15 LPM (20/cs) FDA UDI

Identifiers

Primary DI / UDI-DI
00612479262027 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Nebulizing system delivery set, reusable 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: Nebulizing system delivery set, reusable

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

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d1471ff-6431-4f84-9c2c-2b6501721fb8 33 fields · synced Jun 6, 2026