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2764

Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi

Türkiye · Istanbul Suspended

www.notice.com.tr

Designations

MDR Medical devices · Regulation (EU) 2017/745 Suspended
Conformity assessment annexesAnnex V, Annex II
Designated since2018-01-23
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 1302 - Monitoring devices of vital physiological parameters
  • *MD 0204 - Non-active soft tissue implants
  • *MD 0400 - Non-active dental devices and accessories
  • *MD 0300 - Devices for wound care
  • *MD 0104 - Non-active medical devices with measuring function
  • *MD 1301 - Monitoring devices of non-vital physiological parameters
  • *MD 1400 - Devices for radiation therapy and thermo therapy
  • *MD 0101 - Non-active devices for anaesthesia, emergency and intensive care
  • *MD 0403 - Dental implants
  • *MD 1111 - Software
  • *MD 1402 - Devices utilising non-ionizing radiation
  • *MD 0200 - Non-active implants
  • *MD 0102 - Non-active devices for injection, infusion, transfusion and dialysis
  • *MD 1100 - General active medical devices
  • *MD 0401 - Non-active dental equipment and instruments
  • *MD 0302 - Suture material and clamps
  • *MD 1300 - Monitoring devices
  • *MD 1102 - Respiratory devices, devices including hyperbaric chambers for oxygen therapy, inhalation anaesthesia
  • *MD 1104 - Active surgical devices
  • *MD 0203 - Non-active functional implants
  • *MD 1101 - Devices for extra-corporal circulation, infusion and haemopheresis
  • *MD 0301 - Bandages and wound dressings
  • *MD 0303 - Other medical devices for wound care
  • *MD 0108 - Non-active medical devices for disinfecting, cleaning, rinsing
  • *MD 0402 - Dental materials
  • *MD 0100 - General non-active, non-implantable medical devices
  • *MD 0202 - Non-active orthopaedic implants
MDR Medical devices · Regulation (EU) 2017/745 Suspended
Conformity assessment annexesAnnex V, Annex II
Designated since2018-01-23
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 1302 - Monitoring devices of vital physiological parameters
  • *MD 0204 - Non-active soft tissue implants
  • *MD 0400 - Non-active dental devices and accessories
  • *MD 0300 - Devices for wound care
  • *MD 0104 - Non-active medical devices with measuring function
  • *MD 1301 - Monitoring devices of non-vital physiological parameters
  • *MD 1400 - Devices for radiation therapy and thermo therapy
  • *MD 0101 - Non-active devices for anaesthesia, emergency and intensive care
  • *MD 0403 - Dental implants
  • *MD 1111 - Software
  • *MD 1402 - Devices utilising non-ionizing radiation
  • *MD 0200 - Non-active implants
  • *MD 0102 - Non-active devices for injection, infusion, transfusion and dialysis
  • *MD 1100 - General active medical devices
  • *MD 0401 - Non-active dental equipment and instruments
  • *MD 0302 - Suture material and clamps
  • *MD 1300 - Monitoring devices
  • *MD 1102 - Respiratory devices, devices including hyperbaric chambers for oxygen therapy, inhalation anaesthesia
  • *MD 1104 - Active surgical devices
  • *MD 0203 - Non-active functional implants
  • *MD 1101 - Devices for extra-corporal circulation, infusion and haemopheresis
  • *MD 0301 - Bandages and wound dressings
  • *MD 0303 - Other medical devices for wound care
  • *MD 0108 - Non-active medical devices for disinfecting, cleaning, rinsing
  • *MD 0402 - Dental materials
  • *MD 0100 - General non-active, non-implantable medical devices
  • *MD 0202 - Non-active orthopaedic implants
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=2764

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.