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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

91736042 — Class I MDR by Meyra GmbH

MD Atlas
Meyra GmbH

EUDAMED last updated this device on Apr 28, 2026

91736042

40327662379189

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Meyra GmbH
UDI-DI code: 04032766684077
Reference / catalog number: 91736042

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Manufacturer information

Organization name: Meyra GmbH
SRN: DE-MF-000005780
Manufacturer status: Active

Related devices

1.73640327662379189On the market 9173604640327662379189On the market 1.73640327662379189On the market 1.73540327662645387On the market 990514140327662563282On 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 Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04032766684077
Basic UDI-DI: 40327662379189
Reference / catalog number: 91736042
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: https://www.meyra.de/rollstuehle/active/active-rollstuhl-details/avanti-1736
Clinical sizes: Seat width — 42 MU10

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
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Software identification