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Astrolabe

by Astrolabe - Fabricação de Implantes Médicos, Lda 468 variants

Ref 09.15.08.24004Model Bending Templates

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05600432880130 Basic UDI-DI 05600432880130UDI-DIDate25 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Bending Templates, for Radius Wide Volar-E, Right, 04 Holes
Model / reference
Bending Templates, 09.15.08.24004
Primary DI / UDI-DI
05600432880130
Basic UDI-DI
B-05600432880130
EMDN code
L0922 Orthopaedic surgery guides, reusable
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000016588

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Properties

  • Sterilise before use
  • Reusable

Other properties (10)

  • Supplied sterile: No
  • Implantable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No