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Ochelari De Citit Perspektive ARP101A +1.00

by Amc SRL

Ref ARP101A +1.00Model OCHELARI DE CITIT CU RAMĂ ÎNTREAGĂ, DIN METAL, CU LENTILE DIN PLASTIC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5949285OCHCITRAMINTMETPGZ Basic UDI-DI 05949285005711UDI-DIDate8 May 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Ochelari De Citit Cu Ramă Întreagă, Din Metal, Cu Lentile Din Plastic
Model / Reference
OCHELARI DE CITIT CU RAMĂ ÎNTREAGĂ, DIN METAL, CU LENTILE DIN PLASTIC, ARP101A +1.00
Primary DI / UDI-DI
05949285005711
Basic UDI-DI
5949285OCHCITRAMINTMETPGZ
EMDN Code
Q0210030102 Ready to wear plastic spectacles with organic lenses
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000019035

Other devices from Amc SRL

See all devices from Amc SRL →

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