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Pondus Size 3

by Tyromotion GmbH

Ref 15426Model R1

Pondus Size 3 (15426) is a Class I device made by tyromotion GmbH, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 912007718PONDUSEW), active 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 Number912007718PONDUSEW Basic UDI-DI 09120077180175UDI-DIDate19 May 2026RegisteredStatusActive

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  • Withdrawn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
Pondus
Model / reference
R1, 15426
Primary DI / UDI-DI
09120077180175
Basic UDI-DI
912007718PONDUSEW
Direct marketing DI
09120077180175
EMDN code
Z12069099 Various physiotherapy and rehabilitation instruments - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
AT-MF-000016168

Similar devices in this category

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

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Properties

Other properties (14, all answered No)