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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 air bubble/fluid level detector FDA UDI
Device Name
Level sensors pads are used to attach the level sensors to a hard shell reservoir. Includes coupling gel. FDA UDI
Model / Reference
195240 FDA UDI
Description
Level sensors pads are used to attach the level sensors to a hard shell reservoir. Includes coupling gel. FDA UDI

Identifiers

Catalog Number
195240 FDA UDI
Primary DI / UDI-DI
10886799001704 FDA UDI
510(k) Number
K151349 FDA UDI
FDA Product Code
DTQ FDA UDI
GMDN Term
Cardiopulmonary bypass system air bubble/fluid level detector 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

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 system air bubble/fluid level detector

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 air bubble/fluid level detector.

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 f226e488-5be2-4c4f-85c9-1e5d0d03bc66 35 fields · synced Jun 9, 2026