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Manulacer - S

EUDAMED

Class I (EU MDR)

Ref PO 3119-B SModel PO 3119-B

by Lomed Nederland

Identity

Trade Name
Manulacer - S EUDAMED
Device Name
Manulacer EUDAMED
Model / Reference
PO 3119-B EUDAMED
PO 3119-B S EUDAMED

Identifiers

Primary DI / UDI-DI
08718873001261 EUDAMED
Basic UDI-DI
87188733119BN2 EUDAMED
EMDN Code
Y060612 WRIST-HAND ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Manulacer - S by Lomed Nederland — 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
Lomed Nederland
EUDAMED SRN
NL-MF-000032807

Sources (1)

  • EUDAMED 8df65667-65fc-44d2-b8b1-fb8f0e8b9b79 61 fields · synced Jun 18, 2026