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Terumo® Advanced Perfusion System 1

FDA UDI

Class II (US FDA UDI)

by Terumo Cardiovascular Systems Corporation

Identity

Trade Name
Terumo® Advanced Perfusion System 1 FDA UDI
Generic Name
Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
Device Name
The flow sensor is a non-invasive ultrasonic transducer used to measure fluid flow. Includes ultrasonic coupling gel. FDA UDI
Model / Reference
6382 FDA UDI
Description
The flow sensor is a non-invasive ultrasonic transducer used to measure fluid flow. Includes ultrasonic coupling gel. FDA UDI

Identifiers

Catalog Number
6382 FDA UDI
Primary DI / UDI-DI
00886799000083 FDA UDI
510(k) Number
K151349 FDA UDI
FDA Product Code
DTQ FDA UDI
GMDN Term
Cardiopulmonary bypass system centrifugal pump drive unit 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiopulmonary bypass system centrifugal pump drive unit

Terumo® Advanced Perfusion System 1 by Terumo Cardiovascular Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system centrifugal pump drive unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6604bee-23a4-47fb-9faa-442c071b7239 35 fields · synced Jun 9, 2026