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Centrimag® 24fr Return Cannula Kit

FDA UDI

Class II (US FDA UDI)

by Thoratec Switzerland GmbH

Identity

Trade Name
CENTRIMAG® 24FR RETURN CANNULA KIT FDA UDI
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return FDA UDI
Device Name
24FR RETURN CANNULA KIT FDA UDI
Model / Reference
201-50068 FDA UDI
Description
24FR RETURN CANNULA KIT FDA UDI

Identifiers

Catalog Number
201-50068 FDA UDI
Primary DI / UDI-DI
07640135140191 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return

Centrimag® 24fr Return Cannula Kit by Thoratec Switzerland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thoratec Switzerland GmbH

Sources (1)

  • FDA UDI 74172af5-96a8-4c20-a1b5-972485994b15 36 fields · synced May 30, 2026