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23ga Intuitive Extendable MaxReach- Oertli

EUDAMED

Class IIa (EU MDR)

Ref VK401323

by Vortex Surgical Inc

Identity

Trade Name
23ga Intuitive Extendable MaxReach- Oertli EUDAMED
Device Name
Laser Probe and Illumination Devices EUDAMED
Model / Reference
VK401323 EUDAMED

Identifiers

Primary DI / UDI-DI
00810123483846 EUDAMED
Basic UDI-DI
081012348LaserDX EUDAMED
Unit of Use DI
00810123483761 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

23ga Intuitive Extendable MaxReach- 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 898a23a4-f4a4-45f0-b330-60afc5b25235 61 fields · synced Jul 15, 2026