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HydraFacial

by Hydrafacial, LLC 9 variants

Part of a family of 10 devices: see the family page

Ref 70218Model 74111

HydraFacial (70218) is a Class I device made by Hydrafacial LLC, registered in EUDAMED on 30 Jul 2025 (Basic UDI-DI 081000753TIP9V), 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 Number081000753TIP9V Basic UDI-DI 00810007530895UDI-DIDate30 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  • Withdrawn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
HydroPeel Tip, Large Clear
Model / reference
74111, 70218
Primary DI / UDI-DI
00810007530895
Basic UDI-DI
081000753TIP9V
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

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Other devices from Hydrafacial LLC

See all devices from Hydrafacial LLC →

Properties

Other properties (14, all answered No)