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Sign in to claim this brandScholz Medical GmbH
Germany·DE-MF-000008955
Last updated September 18, 2026
What Scholz Medical GmbH makes
Scholz Medical GmbH produces surgical instruments and consumables for medical procedures, including forceps such as the Magill and Crile-Wood needle holders, as well as specialized tools like the Scharfe-Löffel combination and clamp removers. Their portfolio also includes adhesive dressings, gauze, and compression pads designed for specific surgical sets, such as the Thorax-Chirurgie Set. Additionally, they manufacture ocular and vascular devices, such as the Bangerter cannula and Birkett clamp, alongside lacrimal drainage tubes and knotted cannulae for precise medical applications.
The company’s devices are classified under EU medical device regulations as Class I and Class IIa, reflecting varying levels of risk and regulatory oversight. These products are registered in the EU’s eudamed database, ensuring compliance with European Union medical device directives. Scholz Medical GmbH is based in Germany.
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 Scholz Medical GmbH manufacture?
Scholz Medical GmbH specializes in surgical instruments and medical consumables. Their portfolio includes forceps like the Magill and Crile-Wood needle holders, specialized surgical tools such as clamp removers and Scharfe-Löffel combinations, as well as adhesive dressings, gauze, and compression pads tailored for specific surgical sets like the Thorax-Chirurgie Set. They also produce ocular devices like the Bangerter cannula and Birkett clamp, alongside lacrimal drainage tubes and knotted cannulae for precise medical applications.
Where is Scholz Medical GmbH based?
Scholz Medical GmbH is based in Germany, as indicated by the company’s country designation in regulatory records.
Which regulatory registries list Scholz Medical GmbH’s devices?
Scholz Medical GmbH’s devices are listed in the eudamed database, which is the EU’s central registry for medical devices. This ensures transparency and compliance with European Union medical device regulations.
How are Scholz Medical GmbH’s devices classified under EU regulations?
Scholz Medical GmbH’s devices fall under Class I and Class IIa classifications in the EU. These classifications determine the level of regulatory oversight required, with Class I being lower risk and Class IIa involving additional scrutiny due to higher risk factors. The classification is based on factors like intended use, duration of contact with the body, and potential risks.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Germany
- Address
- 1, Robert-Bosch-Strasse , Bruckmühl, Germany
- Website
- www.scholz-instruments.com
- —
- —
- [email protected]
- Phone
- 080628070801
- PRRC Contact
- —
- EUDAMED SRN
- DE-MF-000008955
- FDA FEI Number
- —
- DUNS Number
- —
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