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: Portable active medical device mount FDA UDI
Device Name: The mounting arm attaches to the APS1 vertically mounting pole and is used as a mount for the Central Control Monitor. FDA UDI
Model / Reference: 90000746 FDA UDI
Description: The mounting arm attaches to the APS1 vertically mounting pole and is used as a mount for the Central Control Monitor. FDA UDI

Identifiers

Catalog Number: 90000746 FDA UDI
Primary DI / UDI-DI: 00886799001820 FDA UDI
510(k) Number: K221895 FDA UDI
FDA Product Code: DTQ FDA UDI
GMDN Term: Portable active medical device mount 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

FDA UDI

Single Use

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable active medical device mount

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

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Cleared under the same submission

K221895 also covers:

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: Terumo Cardiovascular Systems Corporation

Sources (1)

FDA UDI ab0d64cd-ae79-4588-9814-d1a93a57350e 36 fields · synced Jun 9, 2026