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25ga Flex-Tip Illuminated Laser Probe- Oertli

EUDAMED

Class IIa (EU MDR)

Ref VK401215

by Vortex Surgical Inc

Identity

Trade Name
25ga Flex-Tip Illuminated Laser Probe- Oertli EUDAMED
Device Name
Laser Probe and Illumination Devices EUDAMED
Model / Reference
VK401215 EUDAMED

Identifiers

Primary DI / UDI-DI
00810123483822 EUDAMED
Basic UDI-DI
081012348LaserDX EUDAMED
Unit of Use DI
00810123483747 EUDAMED
EMDN Code
Q02040301 OCULAR ENDOPHOTOCOAGULATION FIBERS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

25ga Flex-Tip Illuminated Laser Probe- Oertli by Vortex Surgical, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Vortex Surgical Inc
EUDAMED SRN
US-MF-000022888
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 85846a77-1078-414c-b514-41184e793cee 61 fields · synced Jun 20, 2026