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Emy application

by Fizimed

Ref APP V9Model Emy

Emy application (APP V9) is a medical device (EU MDR Class I; EMDN category pelvic floor rehabilitation devices) made by Fizimed, registered in EUDAMED on 1 Jul 2022 (Basic UDI-DI 377011873EMYJM), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number377011873EMYJM Basic UDI-DI 03770011873074UDI-DIDate1 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  • Withdrawn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, APP V9
Primary DI / UDI-DI
03770011873074
Basic UDI-DI
377011873EMYJM
Direct marketing DI
03770011873074
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)