CentriMag™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name: CentriMag™ FDA UDI
Generic Name: Cardiopulmonary bypass system priming set FDA UDI
Device Name: PRE-CONNECTED PACK FDA UDI
Model / Reference: CMAEK00 FDA UDI
Description: PRE-CONNECTED PACK FDA UDI

Identifiers

Catalog Number: CMAEK00 FDA UDI
Primary DI / UDI-DI: 05415067036414 FDA UDI
510(k) Number: K222297 FDA UDI
FDA Product Code: DTQ FDA UDI
GMDN Term: Cardiopulmonary bypass system priming set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4220 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Cardiopulmonary bypass system centrifugal pump Cardiopulmonary bypass system priming set

CentriMag™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: St. Jude Medical, Inc.

Sources (1)

FDA UDI 2449552b-858a-4b60-ba36-978996cc4a0e 37 fields · synced May 30, 2026