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Manufacturer of orthopedic implants and surgical instruments based in Kladno, Czech Republic since 1992.
ChequiaFundada en 1992Fabricante · SaludISO 13485CE certification (Class I, IIb, III)ISO 9001
catalog
A comprehensive catalog of primary arthroplasty implants including hip, knee, and thumb joint replacement components, detailing materials used such as stainless steel, titanium alloys, CoCrMo, and UHMWPE.
catalog
Catalog and surgical overview for the SF cementless hip stem, detailing design features, material composition (titanium alloy with bioactive plasma coating), and clinical indications for younger patients.
catalog
A catalog detailing the modular hip hemiarthroplasty system developed by Beznoska, including surgical techniques and instrument information, designed for treating intracapsular femoral neck fractures.
catalog
A comprehensive catalog detailing Beznoska's hip, knee, and revision arthroplasty systems, including material specifications and component lists.
catalog
Product catalog and technical overview for the 2nd generation SF cementless hip replacement system, detailing implant materials, design features, indications for use, and surgical compatibility.
certificate ce
EU Quality Management System Certificate issued by 3EC International (Notified Body 2265) to BEZNOSKA, s.r.o. for the ELiS Total Trapezium-Metacarpal Joint Replacement system under Regulation (EU) 2017/745.
certificate ce
EU Technical Documentation Assessment Certificate issued by 3EC International for the ELiS Total Trapezium-Metacarpal Joint Replacement system, confirming compliance with Regulation (EU) 2017/745.
certificate ce
EC Certificate for Full Quality Assurance System issued by Elektrotechnický zkušební ústav for Beznoska, s.r.o. covering the design, manufacturing, and final inspection of ancillary components for the SVR Total Revision Knee Replacement system.
certificate ce
EC Design-Examination Certificate for total knee joint replacement devices, issued by the Electrotechnical Testing Institute (Notified Body No. 1014) to Beznoska, s.r.o. under Directive 93/42/EEC.
certificate ce
EC Certificate for Full Quality Assurance System issued to Beznoska, s.r.o. for the design, manufacturing, and final inspection of Total knee joint replacement (Class III).
certificate ce
EC Certificate for Full Quality Assurance System issued to Beznoska, s.r.o. for the design, manufacturing, and final inspection of hip joint replacement (hemiarthroplasty and ancillary components) class IIb.
certificate ce
EC Design-Examination Certificate for Total hip joint replacement (class III) issued by the Electrotechnical Testing Institute (Notified Body No. 1014) to Beznoska s.r.o. in accordance with Directive 93/42/EEC.
certificate ce
EC Certificate for Full Quality Assurance System issued by the Electrotechnical Testing Institute (EZÚ) to Beznoska, s.r.o. for the design, manufacturing, and final inspection of Total hip joint replacement (Class III).
certificate ce
EC Certificate for Full Quality Assurance System according to Directive 93/42/EEC, Annex II, excluding Section 4, issued by TÜV Rheinland for Changzhou Medical Bioengineering Co., Ltd.
certificate ce
EC Certificate for Production Quality Assurance System under Directive 93/42/EEC Annex V for Disposable Electronically Pulsed Lavage Suction Apparatus.
certificate ce
EU Quality Management System Certificate issued to TEKNIMED SAS under Regulation (EU) 2017/745 (MDR), covering various classes of implantable devices including bone cements, bone substitutes, and osteosynthesis implants.
certificate ce
EU Quality Management System Certificate issued by 3EC International (Notified Body 2265) to BEZNOSKA, s.r.o. for the ELiS Total Trapezium-Metacarpal Joint Replacement system under Regulation (EU) 2017/745.
certificate ce
EU Technical Documentation Assessment Certificate issued by 3EC International for the ELiS Total Trapezium-Metacarpal Joint Replacement system, confirming compliance with Regulation (EU) 2017/745.
certificate iso
ISO 13485:2016 quality management system certificate for Beznoska, s.r.o. covering the design, development, production, and sale of inactive osteo-orthopedic implants and instruments.
clinical evaluation
This document is a Summary of Safety and Clinical Performance (SSCP) for the trapeziometacarpal joint replacement device, providing information on clinical evaluation, safety, and performance data.
ifu
Instructions for use for Beznoska cementless hip stems, including SF, RMD, and Trio models. Covers product descriptions, material specifications (ISO 5832-3, ISO 5832-2, ISO 13779-2, ISO 5832-12), indications, contraindications, surgical warnings, and post-operative care.
certificate other
Ukrainian State Registration Certificate for Beznoska and CeramTec joint implants, including knee, shoulder, and hip joint implants.
ifu
A comprehensive guide defining the symbols used on medical device packaging and labeling, compliant with ISO 15223-1 and ISO 7010 standards.
ifu
A comprehensive guide defining the symbols used on medical device packaging and labeling, compliant with ISO 15223-1 and ISO 7010 standards.