← Back to catalogue

Myah

EUDAMED

Class IIa (EU MDR)

Ref 42-0000983Model MYAH; MYOPIA EXPERT 700

by Visia imaging SRL

Identity

Trade Name
MYAH EUDAMED
Device Name
MYAH EUDAMED
Model / Reference
MYAH; MYOPIA EXPERT 700 EUDAMED
42-0000983 EUDAMED

Identifiers

Primary DI / UDI-DI
08034028770340 EUDAMED
Basic UDI-DI
803402877BIOMETER2C7 EUDAMED
EMDN Code
Z12120123 COMPUTERISED CORNEAL TOPOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Myah by Visia Imaging Srl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Visia imaging SRL
EUDAMED SRN
IT-MF-000015628

Sources (1)

  • EUDAMED 8fdadcf6-c3f5-4378-86d4-a3b695657b78 61 fields · synced Jun 18, 2026