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Sarns™ Cardioplegia Sets

FDA UDI

Class I (US FDA UDI)

by Terumo Cardiovascular Systems Corporation

Identity

Trade Name
Sarns™ Cardioplegia Sets FDA UDI
Generic Name
Portable active medical device mount FDA UDI
Device Name
MP-4 Monitoring Module Holder FDA UDI
Model / Reference
16529701 FDA UDI
Description
MP-4 Monitoring Module Holder FDA UDI

Identifiers

Catalog Number
16529701 FDA UDI
Primary DI / UDI-DI
00886799001561 FDA UDI
FDA Product Code
KRI FDA UDI
GMDN Term
Portable active medical device mount FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4200 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable active medical device mount

Sarns™ Cardioplegia Sets by Terumo Cardiovascular Systems Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable active medical device mount.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 92519c25-dab2-4731-a2a1-4c5faabacef5 35 fields · synced Jun 9, 2026