Bricon
Wurmlingen, Germany
Bricon is a Wurmlingen-based manufacturer of implants and instruments for spine, CMF and trauma surgery.
DAUSCH Medizintechnik
Wurmlingen, Germany
DAUSCH Medizintechnik is a Wurmlingen-based manufacturer of tubular shaft instruments for endoscopic surgery.
Digimed Medizintechnik
Wurmlingen, Germany
Wurmlingen manufacturer of surgical instruments, orthopaedic and maxillofacial implants and sterile container systems.
Günter Stoffel Medizintechnik (INSTO)
Wurmlingen, Germany
Wurmlingen maker of microsurgical and endoscopic instruments under the INSTO name, FDA-listed as a contract manufacturer.
Kreidler Medizintechnik
Wurmlingen, Germany
Wurmlingen family company and contract manufacturer of custom surgical instruments, implants, retractors and trocars.
MICROMED Medizintechnik
Wurmlingen, Germany
MICROMED Medizintechnik is a Wurmlingen-based manufacturer of instruments for electrosurgery, microsurgery and orthopaedic surgery.
MTI Medizin-Technische Instrumente
Wurmlingen, Germany
MTI Medizin-Technische Instrumente is a Wurmlingen-based manufacturer of medical devices and surgical instruments.
Ortho Solutions
Wurmlingen, Germany
Wurmlingen manufacturer of orthopaedic and trauma implants, founded in 2002 and producing exclusively in Germany.
Schmid Medizintechnik
Wurmlingen, Germany
Wurmlingen maker of microsurgical instruments such as micro needle holders, micro forceps and micro scissors.
SIEMA Siegfried Martin
Wurmlingen, Germany
SIEMA Siegfried Martin is a Wurmlingen bei Tuttlingen-based manufacturer of surgical and dental scissors.
TONTARRA Medizintechnik
Wurmlingen, Germany
German company near Tuttlingen developing and producing instruments for open surgery, endoscopy and laminectomy.
Business types in Wurmlingen
Regulation in Germany
Germany is in the EU / EEA, so the EU framework applies.
Regulator: European Commission (DG SANTE) with national competent authorities of EU/EEA Member States
Two EU regulations govern medical devices and IVDs in the EU/EEA; devices need CE marking after the conformity assessment route set by their risk class.
From the sourced EU MDR / IVDR entry, checked 29 October 2026. General information, not legal advice. Requirements for Germany · All medical certifications
Frequently asked questions
How do I search the whole Tuttlingen area, not just Tuttlingen itself?
The directory files companies under the town in their address, so companies in the Tuttlingen area are spread over many city pages. Besides Tuttlingen (more than 50 companies), there are separate pages for Tuttlingen-Nendingen, Wurmlingen (about 10), Emmingen-Liptingen, Neuhausen ob Eck, Rietheim-Weilheim, Seitingen-Oberflacht, Spaichingen, Frittlingen, Mühlheim an der Donau and Fridingen, plus several smaller towns.
Note that "Emmingen" and "Emmingen-Liptingen" are separate pages, as are "Tuttlingen" and "Tuttlingen-Nendingen", so check both. For a single list of all German companies, use the Germany country page.
What must a German importer check when bringing instruments in from outside the EU?
Under Article 13 of the EU MDR, an importer established in the EU, for example a German company buying from a Pakistani or Chinese factory, must verify before placing the device on the market that:
- the device is CE marked and has an EU Declaration of Conformity;
- the manufacturer is identified and has designated an EU authorized representative;
- labeling and instructions for use meet the MDR, and a UDI has been assigned where required.
The importer must add its own name and address to the device, packaging or an accompanying document, register in EUDAMED and keep complaint and traceability records. An importer that changes the labeling or intended purpose may take on manufacturer obligations. Find German importers and distributors on the Germany country page.