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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
Suction system canister liner FDA UDI
Device Name
1000cc Flex Can S/Strt Conn FDA UDI
Model / Reference
65652-613A FDA UDI
Description
1000cc Flex Can S/Strt Conn FDA UDI

Identifiers

Catalog Number
65652-613A FDA UDI
Primary DI / UDI-DI
50885380158580 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Suction system canister liner 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

No

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

Dimensions & Sizes

Size
Total Volume — 1000 Milliliter FDA UDI

Category: Suction system canister liner

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

Similar devices

Also classified as Suction system canister liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12e561f8-e018-4b6b-afc8-6531c1d18936 35 fields · synced Jun 8, 2026