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Compression Tip

by Symbios Orthopédie S.A.

Ref PD000069

Compression Tip (PD000069) is a Class I device made by Symbios Orthopédie S.A., registered in EUDAMED on 22 Jul 2026 (Basic UDI-DI B-07630013663799), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07630013663799 Basic UDI-DI 07630013663799UDI-DIDate22 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Compression Tip
Model / reference
PD000069
Primary DI / UDI-DI
07630013663799
Basic UDI-DI
B-07630013663799
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000020168
Authorised representative
Symbios France SAS FR-AR-000017731

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Symbios Orthopédie S.A.

See all devices from Symbios Orthopédie S.A. →

Properties

  • Sterilise before use
  • Reusable
Other properties (10, all answered No)