DQS Polska Sp. z o.o

🇵🇱 Poland · Warszawa Suspended

Designations

MDR Medical devices · Regulation (EU) 2017/745 Suspended

Conformity assessment annexesAnnex V, Annex II

Designated since2015-08-12

Full scope text from the register

Annexes

Annex V, Annex II

Procedures

EC declaration of conformity (full quality assurance system), EC declaration of conformity (production quality assurance)

Products

*MD 0110 - Non-active medical devices for ingestion
*MD 1111 - Software
*MD 0103 - Non-active orthopaedic and rehabilitation devices
*MD 0106 - Non-active instruments
*MD 0400 - Non-active dental devices and accessories
*MD 0107 - Contraceptive medical devices
*MD 1101 - Devices for extra-corporal circulation, infusion and haemopheresis
*MD 0300 - Devices for wound care
*MD 0402 - Dental materials
*MD 0302 - Suture material and clamps
*MD 0104 - Non-active medical devices with measuring function
*MD 1100 - General active medical devices
*MD 1107 - Active devices for disinfection and sterilisation
*MD 0403 - Dental implants
*MD 0200 - Non-active implants
*MD 0100 - General non-active, non-implantable medical devices
*MD 0108 - Non-active medical devices for disinfecting, cleaning, rinsing
*MD 0401 - Non-active dental equipment and instruments
*MD 0202 - Non-active orthopaedic implants
*MD 0303 - Other medical devices for wound care
*MD 0301 - Bandages and wound dressings
*MD 0102 - Non-active devices for injection, infusion, transfusion and dialysis

Source: EU Single Market Compliance Space (SMCS), retrieved 2026-06-23.
https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/free-search?text=2282

This page is an informational mirror of the official register. It is not affiliated with the European Commission. Always verify the current designation and scope against the official SMCS record before relying on it.