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Organization name
UDI-DI code
Reference / catalog number

240017 — Class I MDR by MARO - Mader, s.r.o.

MD Atlas
MARO - Mader, s.r.o.

EUDAMED last updated this device on May 11, 2026

240017

859420134E24094

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MARO - Mader, s.r.o.
UDI-DI code: 08594201340031
Reference / catalog number: 240017

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Manufacturer information

Organization name: MARO - Mader, s.r.o.
SRN: CZ-MF-000047386
Manufacturer status: Active

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250126859420134DTH250ALOn the market 250122N859420134DTH250ALOn the market 250126N859420134DTH250ALOn the market 250122859420134DTH250ALOn the market 240025859420134E24094On 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 Czechia; available across 3 countries total.

Country	On market since	Until
CzechiaPrimary placement	Oct 1, 2019	Dec 31, 9999
Poland		Dec 31, 9999
Slovakia		Dec 31, 9999

Device identification

Trade name: not provided
UDI-DI code: 08594201340031
Basic UDI-DI: 859420134E24094
Reference / catalog number: 240017
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)

L0908ORTHOPAEDIC AND TRAUMATOLOGICAL TRACTION INSTRUMENTS, REUSABLE

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