Development, manufacturing, and distribution of surgical instruments and medical devices for neurosurgical and diagnostic procedures
WILDmedical GmbH
Tuttlingen, DENew on Amplifa
Medical Technology from Tuttlingen
WILDmedical GmbH is a medical technology company located in Tuttlingen, Baden-Württemberg, at the heart of the German medical technology industry. The company develops, produces, and distributes high-quality medical devices, including the Ventricular Drainage System (Duisburg Needle) for ventriculostomy, disposable biopsies for endoscopic myocardial biopsy, as well as medical drills and hand drill units for neurosurgery. The product range also includes standard surgical instruments such as scalpels, punches, scissors, saws, chisels, loop instruments, forceps, and trephines. All products are developed and manufactured 100% in Germany, utilizing high-quality materials and modern manufacturing processes. Product safety includes laser direct marking of the instruments with GS1 DataMatrix code (UDI) for traceability, as well as validated final cleaning with automated core processes for cleaning, disinfection, and sterilization. As a manufacturer of Class-III medical devices according to MDR, WILDmedical provides constant supply readiness to customers worldwide.
- Site
- Tuttlingen
- Processes
- Laser direct marking of instruments (DataMatrix Code / UDI), Validated final cleaning (Cleaning, Disinfection, Sterilization, automatic core processes), Manufacturing of surgical instruments (Scalpels, Punches, Scissors, Saws, Chisels,, Development and production of medical devices (Disposable Biopsies, Ventricular Drainage Systems,, Laser direct marking with GS1 DataMatrix (UDI), Validated final cleaning of instruments, Worldwide delivery with permanent supply readiness
- Materials
- high-quality materials (not specified), High-Quality Materials (not specified), GS1 DataMatrix Direct Marking, Validated Final Cleaning
- Certificates
- DIN EN ISO 13485:2016, EU QM Certificate MDR (Annex IX Chapter I/III), EU Certificate for Technical Documentation MDR (Annex IX Chapter II)
- Industries
- Medical Technology, Neurosurgery, Cardiology, Hospitals and Medical Practitioners
- 01
Development
- 02
Manufacturing
- 03
Laser Direct Marking (GS1 DataMatrix / UDI)
- 04
Validated Final Cleaning
- 05
Distribution with Permanent Supply Readiness
Materials and Manufacturing Processes
High-Quality Materials (not specified)
Use of high-quality materials under controlled manufacturing conditions to ensure consistently high product performance.
GS1 DataMatrix Direct Marking
Laser direct marking of instruments for traceability and transparency in clinics and practices.
Validated Final Cleaning
Validated, systematized automatic core processes for cleaning, disinfection, and sterilization; the instrument surface is free of manufacturing residues.
Site
Tuttlingen
DECompany Headquarters, Development, Production, and Distribution
- Materials
- High-Quality Materials (unspecified)
- Special lasers for direct marking
- Automated core processes for cleaning, disinfection, and sterilization
Products
Inside the production
Industries
Processes & technical limits
| Processes | Tolerance | Max. part | Weight | Lot size | Materials |
|---|---|---|---|---|---|
| Laser direct marking of instruments (DataMatrix Code / UDI)Surface | – | – | – | – | – |
| Validated final cleaning (Cleaning, Disinfection, Sterilization, automatic core processes)Surface | – | – | – | – | – |
| Manufacturing of surgical instruments (Scalpels, Punches, Scissors, Saws, Chisels,Engineering | – | – | – | – | – |
| Development and production of medical devices (Disposable Biopsies, Ventricular Drainage Systems,Engineering | – | – | – | – | high-quality materials (not specified) |
Additional services
Quality
Medical devices are subject to strict quality assurance requirements – from certification and approval to the quality management of production and processes. This is guaranteed by WILDmedical GmbH.
| Evidence | Tuttlingen |
|---|---|
| DIN EN ISO 13485:2016 | |
| EU QM Certificate MDR (Annex IX Chapter I/III) | |
| EU Certificate for Technical Documentation MDR (Annex IX Chapter II) |