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EyeSuite Myopia

EUDAMED

Class IIa (EU MDR)

Ref 1023815

by Haag-Streit AG

Identity

Device Name
EyeSuite Myopia EUDAMED
Model / Reference
1023815 EUDAMED

Identifiers

Primary DI / UDI-DI
07640132988796 EUDAMED
Basic UDI-DI
764013298MyopiaDJ EUDAMED
EMDN Code
Z12120102 COMPUTERISED OPTICAL BIOMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

EyeSuite Myopia by Haag-Streit 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

Manufacturer
Haag-Streit AG
EUDAMED SRN
CH-MF-000020981
Authorised Representative
Haag-Streit Deutschland GmbH DE-AR-000025462

Sources (1)

  • EUDAMED 4f30060d-442a-40c7-b5b6-0441a087a275 61 fields · synced Jun 18, 2026