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WendyDrive 2

EUDAMED

Class I (EU MDR)

Ref 11000820Model WendyDrive 2Ref 11000720Ref 11000810

by United Care Products B.V.

Identity

Trade Name
WendyDrive 2 EUDAMED
Device Name
WendyDrive2 EUDAMED
Model / Reference
WendyDrive 2 EUDAMED
11000820 EUDAMED
11000720 EUDAMED
11000810 EUDAMED

Identifiers

Primary DI / UDI-DI
08720618143808 EUDAMED
08720618143105 EUDAMED
08720618143815 EUDAMED
Basic UDI-DI
872061814312DF EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS 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

WendyDrive 2 by United Care Products 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-000035901

Sources (3)

  • EUDAMED 79a804ef-8ce6-4c7b-9f52-e7761dfe57c9 61 fields · synced Jul 26, 2026
  • EUDAMED 3a83ad22-20be-4fe5-aa13-b84d37ba516a 61 fields · synced May 17, 2026
  • EUDAMED e33ee933-c92e-4baa-a0c1-d562428c84e9 61 fields · synced May 18, 2026