Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

240010 — 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

240010

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: 08594201340079
Reference / catalog number: 240010

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

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: 08594201340079
Basic UDI-DI: 859420134E24094
Reference / catalog number: 240010
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
Serial number
Software identification

Related devices

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.