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S501 F 3TM Sg Vp BV

by Alliage S/a Indústrias Médico Odontológica 2 variants

Ref 16000004300Model Dental Units

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, self-declared

Class I: no certifier involved

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 Number78995813DentalUnitsXL Basic UDI-DI 07899581341441UDI-DIDate11 Dec 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Dental Units, 16000004300
Primary DI / UDI-DI
07899581341441
Basic UDI-DI
78995813DentalUnitsXL
EMDN Code
V08020101 Generic use electric medical chairs
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
BR-MF-000016681
Authorised representative
ELS SOLUTIONS GDIA - UNIPESSOAL LDA. PT-AR-000026128

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: 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