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Astrolabe

by Astrolabe - Fabricação de Implantes Médicos, Lda 110 variants

Ref 09.80.01.02010Model Minimal Invasive Burr

Active European Union

CE MDD

Valid until

Not listed

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05600432880307 Basic UDI-DI 05600432880307UDI-DIDate22 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  • Withdrawn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
Minimal Invasive Burr Straight Helix, Ø2,0 x 10mm
Model / Reference
Minimal Invasive Burr, 09.80.01.02010
Primary DI / UDI-DI
05600432880307
Basic UDI-DI
B-05600432880307
EMDN Code
L091102 Orthopaedic prostheses reamers and burs, reusable
Device Class
Class IIa
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000016588

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Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No