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Preformed Spasticity Splint LT/L

EUDAMED

Class I (EU MDR)

Ref TH1001-09Model TH1001

by Mediroyal Nordic AB

Identity

Trade Name
Preformed Spasticity Splint LT/L EUDAMED
Device Name
Preformed Spasticity Splint EUDAMED
Model / Reference
TH1001 EUDAMED
TH1001-09 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032900903 EUDAMED
Basic UDI-DI
73400329TH100153 EUDAMED
Direct Marketing DI
07340032900903 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

Preformed Spasticity Splint LT/L 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 8a447fd6-041f-451f-bf3d-51cab81003bd 61 fields · synced Jul 13, 2026