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seca 212

by seca gmbh & co. kg

Ref 2121717009Model MDCMS002memf

seca 212 (2121717009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-04012030007108), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-04012030007108 Basic UDI-DI 04012030007108UDI-DIDate5 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
MDCMS002memf, 2121717009
Primary DI / UDI-DI
04012030007108
Basic UDI-DI
B-04012030007108
EMDN code
V0399 Measurement devices - other
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005469

Similar devices in this category

Other devices filed under MEASUREMENT DEVICES - OTHER.

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Properties

  • Measuring function
Other properties (13, all answered No)