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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

1517738 — Class I MDR by Invacare France…

MD Atlas
Invacare France Operations SAS

EUDAMED last updated this device on Nov 21, 2025

1517738

3662050AluLitePN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Invacare France Operations SAS
UDI-DI code: 03662050000354
Reference / catalog number: 1517738

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Manufacturer information

Organization name: Invacare France Operations SAS
SRN: FR-MF-000006807
Manufacturer status: Active

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EK1685680 and suffix3662050Action1r88On the market EK1685711 and suffix3662050Action1r88On the market EK1685704 and suffix3662050Action1r88On the market EK1685684 and suffix3662050Action1r88On the market EK1685682 and suffix3662050Action1r88On the market

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 France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 03662050000354
Basic UDI-DI: 3662050AluLitePN
Reference / catalog number: 1517738
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y122103PUSH WHEELCHAIRS

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