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Active infusion set for OS 4

EUDAMED

Class IIa (EU MDR)

Ref VV662006Model MD0105.75 Active Infusion Set Single Use

by Oertli Instrumente AG

Identity

Trade Name
Active infusion set for OS 4 EUDAMED
Model / Reference
MD0105.75 Active Infusion Set Single Use EUDAMED
VV662006 EUDAMED

Identifiers

Primary DI / UDI-DI
07630003911565 EUDAMED
Basic UDI-DI
76300039MD010575TT EUDAMED
EMDN Code
Q020499 VITRECTOMY DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Active infusion set for OS 4 by Oertli Instrumente Ag — 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

EUDAMED SRN
CH-MF-000016175
Authorised Representative
Oertli Ophthalmedic Österreich GmbH AT-AR-000003554

Sources (1)

  • EUDAMED 5f424406-d8cc-411c-afa1-51ba889a6e5b 61 fields · synced Jul 9, 2026