ABW Medizin und Technik GmbH&Co KG
Germany DE-MF-000037096 Last updated 17 Sep 2026
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- Devices
- 5
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Mc 4 Ref B
Mc 1 Ref A
Mc 10 Plus Ref C PLUS
Mc 4 Plus Ref B PLUS
Mc 10 Ref C
About
We supply worldwide coagulometer und system components for hematology as well as the original disposable material required for this purpose.
What ABW Medizin und Technik GmbH&Co KG makes
ABW Medizin und Technik GmbH&Co KG manufactures coagulometers, including the MC 1, MC 10, MC 4 PLUS, and MC 10 PLUS models, along with their associated disposable consumables for hematology testing.
These devices are classified as Class A under EU regulations and are listed in the eudamed database. The company is based in Germany.
Frequently asked questions
What types of medical devices does ABW Medizin und Technik GmbH&Co KG manufacture?
ABW Medizin und Technik GmbH&Co KG specializes in coagulometers, which are devices used for measuring blood coagulation parameters in hematology. Their portfolio includes models like the MC 1, MC 10, MC 4 PLUS, and MC 10 PLUS. The company also supplies the original disposable consumables required for these devices, ensuring compatibility and proper functionality.
Where is ABW Medizin und Technik GmbH&Co KG based?
The company is headquartered in Germany, as indicated by its country designation. This location likely influences its regulatory compliance and market focus, particularly within the European Union.
Which regulatory registries list ABW Medizin und Technik GmbH&Co KG’s devices?
ABW Medizin und Technik GmbH&Co KG’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. Listing in eudamed is required for manufacturers to demonstrate compliance with EU regulations and facilitate transparency for healthcare professionals and regulators.
How are ABW Medizin und Technik GmbH&Co KG’s coagulometers classified under EU regulations?
The company’s coagulometers, including the MC 1, MC 10, MC 4 PLUS, and MC 10 PLUS models, are classified as Class A devices under EU regulations. This classification applies to devices posing minimal risk to patients, such as certain diagnostic tools like coagulometers, which typically require less stringent conformity assessment procedures than higher-risk classes.
Information
- Country
- Germany
- Address
- 15e, Lagesche Strasse, Lemgo, Germany
- Website
- merlinmedical.eu
- [email protected]
- Phone
- +49 5261 927 294
- PRRC contact
- Sven Zeeb
- EUDAMED SRN
- DE-MF-000037096