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Lotus XL

EUDAMED

Class I (EU MDR)

Ref 59008270

by Lopital Nederland B.V.

Identity

Trade Name
Lotus XL EUDAMED
Device Name
Lotus XL EUDAMED
Model / Reference
59008270 EUDAMED

Identifiers

Primary DI / UDI-DI
08720256103646 EUDAMED
Basic UDI-DI
872025610364659008270U4 EUDAMED
EMDN Code
Y050201 STANDING SUPPORT GAIT TRAINERS 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

Lotus XL by Lopital Nederland B.V. — 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

EUDAMED SRN
NL-MF-000004372

Sources (1)

  • EUDAMED 23934616-3376-48fd-851a-d41daae76424 61 fields · synced Jul 9, 2026