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Reflex

EUDAMED

Class I (EU MDR)

Ref 51005600

by Lopital Nederland B.V.

Identity

Trade Name
Reflex EUDAMED
Device Name
Reflex EUDAMED
Model / Reference
51005600 EUDAMED

Identifiers

Primary DI / UDI-DI
08720256103004 EUDAMED
Basic UDI-DI
872025610300451005600CA EUDAMED
EMDN Code
Y091203 CHAIRS, TOILET AND SHOWER 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

Reflex 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 e6329d01-7a9f-4652-bb92-fa6946721053 61 fields · synced Jul 14, 2026