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Should'r T3

EUDAMED

Class I (EU MDR)

Ref EB1612BI3

by Orliman, S.L.U.

Identity

Trade Name
SHOULD'R T3 EUDAMED
Device Name
EPAULE BRAS EUDAMED
Model / Reference
EB1612BI3 EUDAMED

Identifiers

Primary DI / UDI-DI
08435025925076 EUDAMED
Basic UDI-DI
84350259ORLSM203114A EUDAMED
EMDN Code
Y060621 SHOULDER ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Should'r T3 by Orliman, S.L.U. — Class I — 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
Orliman, S.L.U.
EUDAMED SRN
ES-MF-000001598

Sources (1)

  • EUDAMED df0c9781-0af9-4cfc-a031-f135e674f7c5 61 fields · synced Jul 29, 2026