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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

301300 — Class I MDR by BEZNOSKA, s.r.o.

MD Atlas
BEZNOSKA, s.r.o.

EUDAMED last updated this device on May 26, 2026

301300

859260200001EG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BEZNOSKA, s.r.o.
UDI-DI code: 08592602104696
Reference / catalog number: 301300

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View device family (Basic UDI)

Manufacturer information

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

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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.

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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: 08592602104696
Basic UDI-DI: 859260200001EG
Reference / catalog number: 301300
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)08592602104696

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UDI-PI DataMatrix

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

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EMDN nomenclature code(s)

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

L091201ORTHOPAEDIC SURGERY RASPS, 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

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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