QA MED Solutions
Denmark DK-MF-000001649 Last updated 21 Oct 2026
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- Devices
- 29
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
CosaOP Ref SS201X06-T/C
CosaOP Ref SS101X05-T/C/M
CosaOP Ref WJ20105
CosaOP Ref SS101X05-B/W/M
CosaOP Ref WJ20104
CosaOP Ref SS101X06-T/C/M
CosaOP Ref SS101X01-B/W/M
CosaOP Ref WJ20102
CosaOP Ref SS101XUT-06
CosaOP Ref SS101XUB-05
CosaOP Ref SS101X04-T/C/M
CosaOP Ref SS101XUB-04
CosaOP Ref SS101XUT-02
CosaOP Ref SS101X02-B/W/M
CosaOP Ref SS201X04-T/C
CosaOP Ref SS201X02-T/C
CosaOP Ref SS101XUT-05
CosaOP Ref SS201X03-T/C
CosaOP Ref SS201X05-T/C
CosaOP Ref SS101XUT-03
CosaOP Ref SS101X02-T/C/M
CosaOP Ref SS201X05-B/W
CosaOP Ref SS101XUT-04
Scrub Suit Ref SS101X01-T/C/M
CosaOP Ref SS101XUB-06
CosaOP Ref SS101X03-T/C/M
CosaOP Ref SS201X02-B/W
CosaOP Ref SS201X03-B/W
CosaOP Ref SS101XUT-01
About
At QA MED Solutions we are experts in legislation on requirements of medicin equipment - MDR. We are your external Quality and Regulatory Department.
What QA MED Solutions makes
QA MED Solutions manufactures the CosaOP, a reusable surgical headlight designed for use in operating rooms to provide focused illumination during procedures.
The CosaOP is classified as a Class I medical device and is listed in the EU’s eudamed registry. The company is based in Denmark.
Frequently asked questions
What types of medical devices does QA MED Solutions manufacture?
QA MED Solutions manufactures the CosaOP, a reusable surgical headlight specifically designed for operating rooms. This device is intended to provide focused illumination during surgical procedures, ensuring clear visibility for medical staff.
Where is QA MED Solutions based?
QA MED Solutions is based in Denmark (DK). The company’s location is relevant for understanding its regulatory context, particularly in the European market.
Which regulatory registries list QA MED Solutions’ devices?
The CosaOP, QA MED Solutions’ device, is listed in the EU’s eudamed registry. This database is used to track medical devices authorised for use within the European Economic Area (EEA).
How are QA MED Solutions’ devices classified under medical device regulations?
The CosaOP is classified as a Class I medical device. This classification is determined by its intended use and risk level, with Class I devices generally posing the lowest risk and often requiring fewer regulatory controls.
What is the primary purpose of the CosaOP device?
The CosaOP is designed to provide focused, adjustable illumination for surgical procedures in operating rooms. Its reusable nature and targeted lighting help improve visibility and precision during medical interventions.
Information
- Country
- Denmark
- Address
- 9, Fynsvej, Middelfart, Denmark
- Website
- www.qamedsolutions.com
- [email protected]
- Phone
- +4553605885
- PRRC contact
- Rikke Nygaard
- EUDAMED SRN
- DK-MF-000001649