MedCheck

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Model / Reference

v4.0.1, MedCheck

Primary DI / UDI-DI

05415062391181

Basic UDI-DI

5415062SC31153082J

Direct Marketing DI

05415062391181

EMDN Code

V92 Medical device software - not included in other classes

Device Class

Class IIa

Special Device Type

Software

Market of Registration

Belgium

EUDAMED SRN

US-MF-000042822

Authorised representative

Pfizer Healthcare Ireland Unlimited Company IE-AR-000037888

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  GUDID on market

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  Class I

  FDA 510(k) K854726 Active Cleared 24 Feb 1986

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  Class II

  FDA 510(k) K780413 Active Cleared 24 Apr 1978

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  Class I

  FDA 510(k) K790089 Active Cleared 6 Mar 1979

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  Class II

  FDA 510(k) K851971 Active Cleared 20 Jun 1985

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