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Medi-Vac

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
MEDI-VAC FDA UDI
Generic Name
Luer/non-ISO80369-standardized linear connector, single-use FDA UDI
Device Name
CRD Flex Advantage 90 Adapter 50/Box FDA UDI
Model / Reference
65652-109 FDA UDI
Description
CRD Flex Advantage 90 Adapter 50/Box FDA UDI

Identifiers

Catalog Number
65652-109 FDA UDI
Primary DI / UDI-DI
20885380131193 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Luer/non-ISO80369-standardized linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer/non-ISO80369-standardized linear connector, single-use

Medi-Vac by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/non-ISO80369-standardized linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae06acdb-c0ab-465e-b486-07b3e594e068 34 fields · synced Jun 8, 2026