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S-scan MSK ReLife

EUDAMED

Class IIa (EU MDR)

Ref 100001840Model 100001

by Esaote S.p.A.

Identity

Trade Name
S-scan MSK ReLife EUDAMED
Model / Reference
100001 EUDAMED
100001840 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304456366 EUDAMED
Basic UDI-DI
805630445ESA.MR0000003.Q2 EUDAMED
EMDN Code
Z11050101 SECTORAL TOMOGRAPHS (FOR TOMOGRAPHIC EXAMINATIONS OF THE EXTREMITIES) 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

S-scan MSK ReLife 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 593768c9-d645-4edb-834c-94907bbc1f3d 61 fields · synced Aug 1, 2026