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Tymo

by Tyromotion GmbH

Ref 15703Model G6

Tymo (15703) is a virtual-display rehabilitation system (EU MDR Class I; FDA Class I; FDA product code BXB, Exerciser, Powered) made by tyromotion GmbH, registered in EUDAMED on 10 Nov 2021 (Basic UDI-DI 912007718TYMOF6) and listed in FDA GUDID since 18 Jun 2024 (UDI-DI 09120077180144), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number09120077180144 UDI-DI Date18 Jun 2024ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number912007718TYMOF6 Basic UDI-DI 09120077180144UDI-DIDate10 Nov 2021RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 912007718TYMOF6 registered 10 Nov 2021 Active
  • FDA GUDID UDI-DI 09120077180144 listed 18 Jun 2024 Listed

Timeline

2 dated events

  1. Registered EUDAMED 912007718TYMOF6
  2. Listed FDA GUDID 09120077180144

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Virtual-display rehabilitation system, non-supportive, clinical
Model / reference
G6 EUDAMED
15703 EUDAMED
6 GUDID
Primary DI / UDI-DI
09120077180144
Basic UDI-DI
912007718TYMOF6
Direct marketing DI
09120077180144
FDA product code
BXB
EMDN code
Z12069099 Various physiotherapy and rehabilitation instruments - other
GMDN term
Virtual-display rehabilitation system, non-supportive, clinical
Device class
Class I
Regulation number
890.5380
EU registration type
Standard device
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
G6
15703
GUDID
6

Manufacturer details

EUDAMED SRN
AT-MF-000016168

Similar devices in this category

Other devices filed under VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER.

Other devices from tyromotion GmbH

See all devices from tyromotion GmbH →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)