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Ophthalmic Reusable Pack

EUDAMED

Class IIa (EU MDR)

Ref FMSR300303Model FMSR100301, FMSR100302, FMSR100303, FMSR100304, FMSR200301, FMSR200302, FMSR200303, FMSR200304, FMSR300301, FMSR300302, FMSR300303、FMSR300304

by Innolcon Medical Technology (Suzhou) Co., Ltd.

Identity

Trade Name
Ophthalmic Reusable Pack EUDAMED
Device Name
Ophthalmic Reusable Pack EUDAMED
Model / Reference
FMSR100301, FMSR100302, FMSR100303, FMSR100304, FMSR200301, FMSR200302, FMSR200303, FMSR200304, FMSR300301, FMSR300302, FMSR300303、FMSR300304 EUDAMED
FMSR300303 EUDAMED

Identifiers

Primary DI / UDI-DI
06972464944524 EUDAMED
Basic UDI-DI
697246494MD03100ORPP001ZG EUDAMED
EMDN Code
Q020680 PHACOEMULSIFICATION DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Ophthalmic Reusable Pack by Innolcon Medical Technology (Suzhou) Co., Ltd. — 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
CN-MF-000012689
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 80c7a53a-b1be-48d8-975d-d1bef19b06ed 61 fields · synced Jun 18, 2026