HydraFacial
by Hydrafacial, LLC 9 variants
Part of a family of 10 devices: see the family page
Ref 70144, 7400000, 74275Model 7000131, 74111
HydraFacial (70144) is a Class I device made by Hydrafacial LLC, registered in EUDAMED on 30 Jul 2025 (Basic UDI-DI 081000753LYM9X), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number081000753LYM9X | Date30 Jul 2025 | StatusActive |
Official records
- EUDAMED public site 081000753LYM9X
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- HydraFacial Lymphatic KitsHydroPeel Tip, Large Clear
- Model / reference
- 7000131, 70144, 74111, 7400000, 74275
- Primary DI / UDI-DI
- 00810007532127, 00810007531045, 00810007530932, 00810007530901
- Basic UDI-DI
- 081000753LYM9X, 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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