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HydraFacial

by Hydrafacial, LLC 9 variants

Ref 70185

HydraFacial (70185) is a Class I device made by Hydrafacial LLC, registered in EUDAMED on 29 Jul 2025 (Basic UDI-DI 081000753CAP6G), active as of 23 Oct 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081000753CAP6G Basic UDI-DI 00810007531328UDI-DIDate29 Jul 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
HydraFacial Cleaning Caps
Model / reference
70185
Primary DI / UDI-DI
00810007531328
Basic UDI-DI
081000753CAP6G
EMDN code
Z12040299 General medicine therapeutic treatment instruments - other
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
US-MF-000004431
Authorised representative
E C REP LIMITED IE-AR-000003995

Similar devices in this category

Other devices filed under GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER.

Other devices from Hydrafacial LLC

See all devices from Hydrafacial LLC →

Properties

Other properties (14, all answered No)