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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Oxygen quick-connect coupling, male FDA UDI
Device Name
ADAPTER,OXY,DISS MALE,1/4" HOSE BARB FDA UDI
Model / Reference
RTMDMOXYB4 FDA UDI
Description
ADAPTER,OXY,DISS MALE,1/4" HOSE BARB FDA UDI

Identifiers

Catalog Number
RTMDMOXYB4 FDA UDI
Primary DI / UDI-DI
10193489026160 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Oxygen quick-connect coupling, male FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

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 quick-connect coupling, male

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen quick-connect coupling, male.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6795f85b-acc1-47b0-a993-99ce5f83c41e 35 fields · synced Jun 8, 2026