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Raszpla

by ChM spółka z ograniczoną odpowiedzialnością 45 variants

Part of a family of 45 devices: see the family page

Ref 40.6806.012Model BONE RASP

Raszpla (40.6806.012) is a Class I device made by ChM spółka z ograniczoną odpowiedzialnością, registered in EUDAMED on 4 Oct 2024 (Basic UDI-DI 59084472NL048MP), active as of 24 Oct 2026.

Active European Union

CE MDR

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/MDR Number59084472NL048MP Basic UDI-DI 05908447386808UDI-DIDate4 Oct 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Raszpla
Model / reference
BONE RASP, 40.6806.012
Primary DI / UDI-DI
05908447386808
Basic UDI-DI
59084472NL048MP
EMDN code
L091002 Instruments for processing materials for osteosynthesis, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000002121

Related devices

Category: Wire holding/twisting forceps

Similar devices in this category

Other devices filed under INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from ChM spółka z ograniczoną odpowiedzialnością

See all devices from ChM spółka z ograniczoną odpowiedzialnością →

Properties

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