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Organization name
UDI-DI code
Reference / catalog number

20532 — Class I MDR by ORTOSERVIS s.r.o.

MD Atlas
ORTOSERVIS s.r.o.

EUDAMED last updated this device on May 20, 2026

20532

859420944004JT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ORTOSERVIS s.r.o.
UDI-DI code: 08594209440054
Reference / catalog number: 20532

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Manufacturer information

Organization name: ORTOSERVIS s.r.o.
SRN: CZ-MF-000003866
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW999
Kontraindikace: Osoby nižší než 150 cm a vyšší než 200 cm, osoby se sníženou mentální schopností chápat rizika spojená s pohybem v chodítku, osoby s hmotností nad 150 kg.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594209440054
Basic UDI-DI: 859420944004JT
Reference / catalog number: 20532
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: Zdravotnický prostředek chodítko STABILO G3 GF se používá pro nácvik stoje a chůze, k rehabilitaci dolních končetin a jako pomocník při chůzi osob se sníženou pohyblivostí. Chodítko je tvořeno kovovou konstrukcí se čtyřmi kolečky. Zadní kolečka jsou doplněna nášlapnými brzdami. Je vybaveno opěrnou deskou, o kterou se uživatel může opřít a dále nastavitelnými madly pro ruce. Opěrná deska je výškově nastavitelná pomocí plynové pružiny s možností pevné aretace. Chodítko slouží k použití na rovných plochách a šikmých plochách, jejichž sklon nepřesahuje 3,5° (rampy). Chodítko je určeno jak k použití uvnitř budov, tak venku na hladkém a zpevněném povrchu.
Additional information URL: No additional information URL provided by the manufacturer.
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
Expiration date
Manufacturing date
Serial number
Software identification

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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.