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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

009-09777 — Class I MDR by Winncare Nordic

MD Atlas
Winncare Nordic

EUDAMED last updated this device on Mar 9, 2026

009-09777

5740008105010T8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Winncare Nordic
UDI-DI code: 05740008100696
Reference / catalog number: 009-09777

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Manufacturer information

Organization name: Winncare Nordic
SRN: DK-MF-000002147
Manufacturer status: Active

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Denmark; available across 1 country total.

Placed on the market in Denmark; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05740008100696
Basic UDI-DI: 5740008105010T8
Reference / catalog number: 009-09777
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Intended for use in lifting or transferring people with reduced mobility.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 68 cm x 100 cm

EMDN nomenclature code(s)

V08050399PATIENT TRANSFER LIFTS - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification