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4474-03 : 20g/25g (0.9/0.5mm) Perflurocarbon Co-Axial Cannula

EUDAMED

Class IIa (EU MDR)

Ref 4474-03

by Sterimedix Ltd

Identity

Device Name
4474-03 : 20g/25g (0.9/0.5mm) Perflurocarbon Co-Axial Cannula EUDAMED
Model / Reference
4474-03 EUDAMED

Identifiers

Primary DI / UDI-DI
D-5056030401275QL EUDAMED
Basic UDI-DI
B-5056030401275QL EUDAMED
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

4474-03 : 20g/25g (0.9/0.5mm) Perflurocarbon Co-Axial Cannula by Sterimedix Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Sterimedix Ltd
EUDAMED SRN
GB-MF-000011604
Authorised Representative
Bausch & Lomb GmbH DE-AR-000006810

Sources (1)

  • EUDAMED 56f09bb0-7eec-4c4a-a419-6cfa8a980fb9 61 fields · synced Oct 6, 2026