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MyLab 8 eXP

EUDAMED

Class IIa (EU MDR)

Ref 101620050Model 6200

by Esaote S.p.A.

Identity

Trade Name
MyLab 8 eXP EUDAMED
Model / Reference
6200 EUDAMED
101620050 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304452986 EUDAMED
Basic UDI-DI
B-08056304452986 EUDAMED
EMDN Code
Z11040104 MULTIDISCIPLINARY ULTRASOUND SCANNERS (INTERNAL AND CARDIOLOGY, ETC.) 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

MyLab 8 eXP by Esaote S.p.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Esaote S.p.A.
EUDAMED SRN
IT-MF-000019024

Sources (1)

  • EUDAMED c1c5f9d3-8735-4a82-8741-ab93fc21dc26 61 fields · synced Jun 18, 2026