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Ajl Ocular

by Ajl Ophthalmic, S.a 6 variants

Ref SF-S-AJL, PROCUL-L-AJL, CF-S-AJL, CF-L-AJL

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number84351943012S6 Basic UDI-DI Date23 Apr 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  • Withdrawn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

Device Name
Anillo Simbléfaron
Protector Ocular
Conformador Perforado
Model / Reference
SF-S-AJL, PROCUL-L-AJL, CF-S-AJL, CF-L-AJL
Primary DI / UDI-DI
08435194320849, 08435194320832, 08435194320788, 08435194320801
Basic UDI-DI
84351943012S6, 84351943020S5, 84351943018SJ
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000267

Other devices from Ajl Ophthalmic, S.a

See all devices from Ajl Ophthalmic, S.a →

Properties

  • Sterile

Other properties (12)

  • 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