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Stern-M

by Yanga S.r.L

Ref REDISTERN

Stern-M (REDISTERN) is a Class I device made by Yanga S.r.L, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 80339542921R7), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80339542921R7 Basic UDI-DI 08033954291400UDI-DIDate29 Oct 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  • Withdrawn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
Redistern
Model / reference
REDISTERN
Primary DI / UDI-DI
08033954291400
Basic UDI-DI
80339542921R7
EMDN code
Y060307 Thoracic orthoses
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000053742

Similar devices in this category

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Properties

  • Reprocessed single-use device
Other properties (13, all answered No)