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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

DK1640970 and suffix — Class I MDR by Invacare France…

MD Atlas
Invacare France Operations SAS

EUDAMED last updated this device on Jan 23, 2026

DK1640970 and suffix

3662050Action1r88

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Invacare France Operations SAS
UDI-DI code: 03662050150042
Reference / catalog number: DK1640970 and suffix

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Manufacturer information

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

Related devices

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.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03662050150042
Basic UDI-DI: 3662050Action1r88
Reference / catalog number: DK1640970 and suffix
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)

Y122106REAR SELF-PROPELLED 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
Serial number
Software identification