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RFLSPSD0

by bredent medical GmbH & Co. KG

Ref RFLSPSD0Model system RFLL P-stetic-SD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EBRMSystRePSD0XW Basic UDI-DI +EBRMRFLSPSD00EUDI-DIDate9 Jun 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  • Withdrawn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
system RFLL P-stetic-SD, RFLSPSD0
Primary DI / UDI-DI
+EBRMRFLSPSD00E
Basic UDI-DI
++EBRMSystRePSD0XW
EMDN Code
L159099 Odontostomatology instruments, reusable - other
Device Class
Class IIa
Medical Purpose
Dental restoration

Manufacturer details

EUDAMED SRN
DE-PR-000014118

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Properties

Other properties (1)

  • Sterile: No