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QA MED Solutions

Denmark DK-MF-000001649 Last updated 21 Oct 2026

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Devices
29
Registries
EUDAMED
FDA recalls
0

Catalogue29

  • CosaOP Ref SS201X06-T/C

    Class I EUDAMED Active

  • CosaOP Ref SS101X05-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref WJ20105

    Class I EUDAMED Active

  • CosaOP Ref SS101X05-B/W/M

    Class I EUDAMED Active

  • CosaOP Ref WJ20104

    Class I EUDAMED Active

  • CosaOP Ref SS101X06-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref SS101X01-B/W/M

    Class I EUDAMED Active

  • CosaOP Ref WJ20102

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-06

    Class I EUDAMED Active

  • CosaOP Ref SS101XUB-05

    Class I EUDAMED Active

  • CosaOP Ref SS101X04-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref SS101XUB-04

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-02

    Class I EUDAMED Active

  • CosaOP Ref SS101X02-B/W/M

    Class I EUDAMED Active

  • CosaOP Ref SS201X04-T/C

    Class I EUDAMED Active

  • CosaOP Ref SS201X02-T/C

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-05

    Class I EUDAMED Active

  • CosaOP Ref SS201X03-T/C

    Class I EUDAMED Active

  • CosaOP Ref SS201X05-T/C

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-03

    Class I EUDAMED Active

  • CosaOP Ref SS101X02-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref SS201X05-B/W

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-04

    Class I EUDAMED Active

  • Scrub Suit Ref SS101X01-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref SS101XUB-06

    Class I EUDAMED Active

  • CosaOP Ref SS101X03-T/C/M

    Class I EUDAMED Active

  • CosaOP Ref SS201X02-B/W

    Class I EUDAMED Active

  • CosaOP Ref SS201X03-B/W

    Class I EUDAMED Active

  • CosaOP Ref SS101XUT-01

    Class I EUDAMED Active

About

At QA MED Solutions we are experts in legislation on requirements of medicin equipment - MDR. We are your external Quality and Regulatory Department.

Translated from the manufacturer's own website. Source

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.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

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.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Denmark
Address
9, Fynsvej, Middelfart, Denmark
Phone
+4553605885
PRRC contact
Rikke Nygaard
EUDAMED SRN
DK-MF-000001649