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Astrolabe

by Astrolabe - Fabricação de Implantes Médicos, Lda 468 variants

Ref 09.17.02.00005, 09.05.19.00000Model Inserter, Saw Guide Block

Astrolabe (09.17.02.00005) is a Class I device made by Astrolabe - Fabricação de Implantes Médicos, Lda, registered in EUDAMED on 25 May 2026 (Basic UDI-DI 56004328111080999000002VP), active as of 24 Oct 2026.

Active European Union

CE MDR 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number56004328111080999000002VP Basic UDI-DI 05600432879158UDI-DIDate25 May 2026RegisteredStatusActive
European UnionCE/MDR Number56004328111080999000002VP Basic UDI-DI 05600432879158UDI-DIDate25 May 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 56004328111080999000002VP — open Devices and search for it

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Inserter
Othos Saw Guide Block
Model / reference
Inserter, 09.17.02.00005, Saw Guide Block, 09.05.19.00000
Primary DI / UDI-DI
05600432879158
Basic UDI-DI
56004328111080999000002VP, B-05600432879158
EMDN code
L0999, L0922
Device class
Class I
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000016588

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY GUIDES, REUSABLE.

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Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)