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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

WALKER AIR BLACK. — Class I MDR by FABRICACIONES…

MD Atlas
FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

EUDAMED last updated this device on Mar 16, 2026

WALKER AIR BLACK.

84356695012VR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FABRICACIONES ORTOPEDICAS ALBACETE, S.L.
UDI-DI code: 08436533431431
Reference / catalog number: 0601.0015

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Manufacturer information

Organization name: FABRICACIONES ORTOPEDICAS ALBACETE, S.L.
SRN: ES-MF-000004660
Manufacturer status: Active

Related devices

0611.200184356695013VTOn the market 0611.000184356695013VTOn the market 0611.100184356695013VTOn the market 0611.020184356695013VTOn the market 0611.020284356695013VTOn 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.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: WALKER AIR BLACK.
UDI-DI code: 08436533431431
Basic UDI-DI: 84356695012VR
Reference / catalog number: 0601.0015
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://fortasl.es/es/manuales/?s=air
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y120606WHEELED WALKER

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
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