← Back to catalogue

Multiple Pinhole Occluder

EUDAMED

Class I (EU MDR)

Ref 12130

by Gulden Ophthalmics

Identity

Trade Name
Multiple Pinhole Occluder EUDAMED
Device Name
Occluders EUDAMED
Model / Reference
12130 EUDAMED

Identifiers

Primary DI / UDI-DI
+B091121300Q EUDAMED
Basic UDI-DI
++B091Occluders84 EUDAMED
EMDN Code
Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Multiple Pinhole Occluder by Gulden Ophthalmics — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Gulden Ophthalmics
EUDAMED SRN
US-MF-000008608
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 94fe9f39-cfb9-4bf0-9e74-4d167b59cc2b 61 fields · synced Jul 21, 2026