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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Vacuum quick-connect coupling, female FDA UDI
Device Name
COUPLER,VAC,P-B FEMALE,DISS MALE NO CHK FDA UDI
Model / Reference
RTMPFVACDM FDA UDI
Description
COUPLER,VAC,P-B FEMALE,DISS MALE NO CHK FDA UDI

Identifiers

Catalog Number
RTMPFVACDM FDA UDI
Primary DI / UDI-DI
10193489027082 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Vacuum quick-connect coupling, female 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: Vacuum quick-connect coupling, female

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

Similar devices

Also classified as Vacuum quick-connect coupling, female.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5777e1be-135c-4067-a446-3817fbee5da1 35 fields · synced May 31, 2026