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Swiss Bi-Manual I/A System curved / 23G Aeroplane

EUDAMED

Class IIa (EU MDR)

Ref RIAB23CRModel SMS390S

by Medicel AG

Identity

Trade Name
Swiss Bi-Manual I/A System curved / 23G Aeroplane EUDAMED
Device Name
Swiss Coaxial I/A System Soft Tip angled 45° / 21G EUDAMED
Model / Reference
SMS390S EUDAMED
RIAB23CR EUDAMED

Identifiers

Primary DI / UDI-DI
07630055242877 EUDAMED
Basic UDI-DI
076300552IA03YX EUDAMED
Direct Marketing DI
07630055242877 EUDAMED
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Swiss Bi-Manual I/A System curved / 23G Aeroplane by Medicel AG — Class IIa — MDR — 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/MDR

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Manufacturer

Manufacturer
Medicel AG
EUDAMED SRN
CH-MF-000016652
Authorised Representative
Rudolf Riester GmbH DE-AR-000015844

Sources (1)

  • EUDAMED af524421-8eae-441b-864a-530c2217225a 61 fields · synced Oct 6, 2026