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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

EK1685710 and suffix — Class I MDR by Invacare France…

MD Atlas
Invacare France Operations SAS

EUDAMED last updated this device on Mar 18, 2026

EK1685710 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: 03662050468727
Reference / catalog number: EK1685710 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

Critical warnings

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

CW010
Consult instructions for use

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: 03662050468727
Basic UDI-DI: 3662050Action1r88
Reference / catalog number: EK1685710 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

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.