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Anti-Spasticity splint LT/M

EUDAMED

Class I (EU MDR)

Ref TH1000-08Model TH1000

by Mediroyal Nordic AB

Identity

Trade Name
Anti-Spasticity splint LT/M EUDAMED
Device Name
Anti-Spasticity splint EUDAMED
Model / Reference
TH1000 EUDAMED
TH1000-08 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032900835 EUDAMED
Basic UDI-DI
73400329TH10004Z EUDAMED
Direct Marketing DI
07340032900835 EUDAMED
EMDN Code
Y060613 WRIST-HAND-FINGERS ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Anti-Spasticity splint LT/M by Mediroyal Nordic AB — 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
Mediroyal Nordic AB
EUDAMED SRN
SE-MF-000007821

Sources (1)

  • EUDAMED c45204e5-7c02-4bd4-af38-c97f99fbddd2 61 fields · synced Jul 8, 2026