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Curapuls 670

by Enraf-Nonius B.V.

Ref 1670901

Curapuls 670 (1670901) is a Class IIa device made by Enraf-Nonius B.V., registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-08720618311047), 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-08720618311047 Basic UDI-DI 08720618311047UDI-DIDate16 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
1670901
Primary DI / UDI-DI
08720618311047
Basic UDI-DI
B-08720618311047
EMDN code
Z120609 Shortwave therapy equipment
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000000429

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Properties

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