Skip to content

Dr.GRAM YBS-0181(50)(S)

by Dr.GRAM

Ref YBS-0181(50)(S)

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 Number880026212DRGRAM001ZW Basic UDI-DI 08800262123965UDI-DIDate24 Oct 2024RegisteredStatusActive

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  • Withdrawn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
Spectacle Frame
Model / Reference
YBS-0181(50)(S)
Primary DI / UDI-DI
08800262123965
Basic UDI-DI
880026212DRGRAM001ZW
EMDN Code
Q02100201 Metal spectacle frames without lenses
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
KR-MF-000044678
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Dr.GRAM

See all devices from Dr.GRAM →

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