← Back to catalogue

Sterile Light Fibers

EUDAMED

Class IIa (EU MDR)

Ref LF23.D03

by VitreQ B.V.

Identity

Device Name
Sterile Light Fibers EUDAMED
Model / Reference
LF23.D03 EUDAMED

Identifiers

Primary DI / UDI-DI
08719214222130 EUDAMED
Basic UDI-DI
871921422990GG EUDAMED
EMDN Code
Z1212020785 PHACO-VITRECTOMY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Phacoemulsification system handpiece tip, single-use

Sterile Light Fibers by Vitreq B.V. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification system handpiece tip, single-use.

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
VitreQ B.V.
EUDAMED SRN
NL-MF-000000424

Sources (1)

  • EUDAMED 6102a997-76b4-4e18-a7d1-7284515f1a34 61 fields · synced Jul 10, 2026