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Physisonic ES-7

by Enraf-Nonius B.V.

Ref 0631910Model Physisonic ES-7

Physisonic ES-7 (0631910) is a Class IIa device made by Enraf-Nonius B.V., registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-08720618311252), 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-08720618311252 Basic UDI-DI 08720618311252UDI-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  • Withdrawn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
Physisonic ES-7, 0631910
Primary DI / UDI-DI
08720618311252
Basic UDI-DI
B-08720618311252
EMDN code
Z120610 Ultrasound 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

Other properties (12, all answered No)