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Emy Trainer

by Fizimed

Ref Emy EG, Emy EHModel Emy

Emy Trainer (Emy EG), a medical device (EU MDR Class I; EMDN category pelvic floor rehabilitation devices) made by Fizimed, was registered in EUDAMED on 1 Jul 2022 (Basic UDI-DI 377011873EMYJM); registry data as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number377011873EMYJM Basic UDI-DI Date1 Jul 2022RegisteredStatusActive

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  • Withdrawn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
Emy
Model / reference
Emy, Emy EG, Emy EH
Primary DI / UDI-DI
03770011873081, 03770011873104
Basic UDI-DI
377011873EMYJM
Direct marketing DI
03770011873081
03770011873104
EMDN code
U070399 Pelvic floor rehabilitation devices - other
Device class
Class I
Special device type
Software
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000011804

Similar devices in this category

Other devices filed under PELVIC FLOOR REHABILITATION DEVICES - OTHER.

Other devices from Fizimed

Properties

Other properties (14, all answered No)