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70231-30-01

by Professional Products, Inc.

Ref 70231-30-01Model DSO

70231-30-01 is a Class I device made by Professional Products, Inc., registered in EUDAMED on 6 Mar 2026 (Basic UDI-DI 088369170231FB), withdrawn as of 24 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 Number088369170231FB Basic UDI-DI 08836912620140UDI-DIDate6 Mar 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Model / reference
DSO, 70231-30-01
Primary DI / UDI-DI
08836912620140
Basic UDI-DI
088369170231FB
EMDN code
Y06120601 Passive ankle-foot orthoses
Device class
Class I
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
US-MF-000019828
Authorised representative
MDSS GmbH DE-AR-000005430

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Properties

Other properties (14, all answered No)