358075

Organization name

BEZNOSKA, s.r.o.

SRN

CZ-MF-000000543

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

3 warnings recorded — scroll inside the panel to see all entries.

• CW001

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.

Primary placement in Czechia; available across 2 countries total.

Trade name

not provided

UDI-DI code

08592602125950

Basic UDI-DI

859260202001EW

Reference / catalog number

358075

Issuing entity

GS1

Risk category

Class III

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

The medical devices are intended for knee arthroplasty - replacement of a destroyed joint with an artificial implant - endoprosthesis in the variant with preservation of the posterior cruciate ligament, without preservation of the posterior cruciate ligament or with ligament instability for patients with completed skeletal growth. The goal of total knee arthroplasty is to restore the anatomic axis of the lower extremity, provide joint stability, improve limb function, and eliminate pain.

Additional information URL

https://beznoska.com/eifu

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• P090903020202BICOMPARTMENTAL PRIMARY IMPLANT FIXED BEARING TIBIAL INSERTS