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Td1000

EUDAMED

Class I (EU MDR)

Ref TD1000/ORT5000B/ORT5000CModel Orthopaedic traction device

by Lojer Oy

Identity

Trade Name
TD1000 EUDAMED
Model / Reference
Orthopaedic traction device EUDAMED
TD1000/ORT5000B/ORT5000C EUDAMED

Identifiers

Primary DI / UDI-DI
06430021930828 EUDAMED
Basic UDI-DI
643002193OTA0001Y2 EUDAMED
Direct Marketing DI
06430021930828 EUDAMED
EMDN Code
Z12011280 PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Td1000 by Lojer Oy — 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
Lojer Oy
EUDAMED SRN
FI-MF-000001639

Sources (1)

  • EUDAMED bf673815-daed-4e08-bd8c-ea781fc2a007 61 fields · synced Jul 26, 2026