Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

304735 — Class I MDR by BEZNOSKA, s.r.o.

MD Atlas
BEZNOSKA, s.r.o.

EUDAMED last updated this device on May 26, 2026

304735

859260200001EG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BEZNOSKA, s.r.o.
UDI-DI code: 08592602107864
Reference / catalog number: 304735

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?

View device family (Basic UDI)

Manufacturer information

Organization name: BEZNOSKA, s.r.o.
SRN: CZ-MF-000000543
Manufacturer status: Active

Related devices

304002859260200001EGOn the market 330901B-08592602119553On the market 330902B-08592602119560On the market 330951B-08592602119799On the market 330903B-08592602119577On the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement		Still on market
Slovakia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08592602107864
Basic UDI-DI: 859260200001EG
Reference / catalog number: 304735
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: Reusable surgical instruments are intended to perform special procedures in orthopaedics, surgery and traumatology.
Additional information URL: https://beznoska.com/eifu
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08592602107864

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

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

L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER

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

Become a partner of MD Atlas

Certificates

Certificate health across this manufacturer's portfolio.

2026-MDR/TD-018Issued
Technical documentationNotified body: 2265Expiry: Mar 5, 2031
2026-MDR/QS-018Issued
Quality management systemNotified body: 2265Expiry: Mar 5, 2031
2023-MDR/TD-005/ASupplemented
Technical documentationNotified body: 2265Expiry: May 12, 2028
2023-MDR/QS-005/ASupplemented
Quality management systemNotified body: 2265Expiry: May 12, 2028