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SmartDiagnost

by Philips Medical Systems DMC GmbH

Part of a family of 7 devices: see the family page

Ref 712038

SmartDiagnost (712038) is a Class IIb device made by Philips Medical Systems DMC GmbH, registered in EUDAMED on 12 Jun 2024 (Basic UDI-DI 0884838BM440SS), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0884838BM440SS Basic UDI-DI 00884838132979UDI-DIDate12 Jun 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Fixed Rad-System
Model / reference
712038
Primary DI / UDI-DI
00884838132979
Basic UDI-DI
0884838BM440SS
EMDN code
Z11039099 Various radiodiagnostic and interventional instruments – other
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
DE-MF-000005362

Similar devices in this category

Other devices filed under VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS – OTHER.

Other devices from Philips Medical Systems DMC GmbH

See all devices from Philips Medical Systems DMC GmbH →

Properties

Other properties (14, all answered No)