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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

0032141-007-020 — Class I MDR by DZO s.r.o.

MD Atlas
DZO s.r.o.

EUDAMED last updated this device on Sep 23, 2025

0032141-007-020

859405200222FK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DZO s.r.o.
UDI-DI code: 08594052006322
Reference / catalog number: 0032141-007-020

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View device family (Basic UDI)

Manufacturer information

Organization name: DZO s.r.o.
SRN: CZ-MF-000037146
Manufacturer status: Active

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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.

Critical warnings

No critical warnings reported for this device.

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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: 08594052006322
Basic UDI-DI: 859405200222FK
Reference / catalog number: 0032141-007-020
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: 019T modrá - reflex
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: modrá, reflex+tm.podešev
EU 23

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y063303READY-MADE ORTHOTIC SHOES

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

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