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MyLabOmega eXP

EUDAMED

Class IIa (EU MDR)

Ref 101740044Model 7400

by Esaote S.p.A.

Identity

Trade Name
MyLabOmega eXP EUDAMED
Model / Reference
7400 EUDAMED
101740044 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304455994 EUDAMED
Basic UDI-DI
805630445ESA.US0000005.Y7 EUDAMED
EMDN Code
Z11040103 PORTABLE ULTRASOUND SCANNERS 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

MyLabOmega eXP by Esaote S.p.A. — 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
Esaote S.p.A.
EUDAMED SRN
IT-MF-000019024

Sources (1)

  • EUDAMED 3cf33d55-69f8-487d-b5d1-a88dc3104802 61 fields · synced Jul 29, 2026