Skip to content

MiniMIS Raspel 11

by Falcon Medical Medizinische Spezialprodukte GmbH

Ref 10-4090-011Model Instrumente IIa Raspel Metall

Active European Union

CE MDR

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/MDR Number9010021-02-01-00100000TX Basic UDI-DI 09010098002528UDI-DIDate23 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
Instrumente IIa Raspel Metall, 10-4090-011
Primary DI / UDI-DI
09010098002528
Basic UDI-DI
9010021-02-01-00100000TX
EMDN Code
L091201 Orthopaedic surgery rasps, reusable
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000001607

Other devices from Falcon Medical Medizinische Spezialprodukte GmbH

See all devices from Falcon Medical Medizinische Spezialprodukte GmbH →

Properties

  • Reusable

Other properties (12)

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