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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 mounting unit FDA UDI
Device Name
Cable used to connect the data module to the intended device. FDA UDI
Model / Reference
804982 FDA UDI
Description
Cable used to connect the data module to the intended device. FDA UDI

Identifiers

Catalog Number
804982 FDA UDI
Primary DI / UDI-DI
00886799000847 FDA UDI
510(k) Number
K151349 FDA UDI
FDA Product Code
DWB FDA UDI
DTQ FDA UDI
GMDN Term
Cardiopulmonary bypass system mounting unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4370 FDA UDI
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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiopulmonary bypass system mounting 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 mounting unit.

Cleared under the same submission

K151349 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Cardiovascular Systems Corporation

Sources (1)

  • FDA UDI 39cd4ec6-d0de-4686-8f0e-4ae805907e2e 35 fields · synced Jun 9, 2026