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RegJoint sizer

by Scaffdex Oy 6 variants

Ref S01, RG0003, RG0005, RG0004, RG0007, S06

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06430047220217 Basic UDI-DI Date20 Dec 2021RegisteredStatusActive

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  • Withdrawn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

Trade Name
RegJoint sizer
RegJoint
Model / Reference
S01, RG0003, RG0005, RG0004, RG0007, S06
Primary DI / UDI-DI
06430047220217, 06430047220033, 06430047220057, 06430047220040, 06430047220071, 06430047220262
Basic UDI-DI
B-06430047220217, B-06430047220033, B-06430047220057, B-06430047220040, B-06430047220071, B-06430047220262
EMDN Code
L091199, P900402
Device Class
Class I
Class III
EU market of registration
Germany
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000012283

Other devices from Scaffdex Oy

See all devices from Scaffdex Oy →

Properties

  • Sterile NoEUDAMEDYesEUDAMED
  • Implantable NoEUDAMEDYesEUDAMED
  • Reusable YesEUDAMEDNoEUDAMED

Other properties (8)

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