Medical Devices
High-speed medical production
With more than 30 years of experience in thermoplastics joining technologies, Weidmann Medical is a trusted manufacturer of medical device components. We offer multi-component molding, plastics welding, fully automated assembly lines, in-line quality control, and labeling – providing reliable, high-speed solutions tailored to the needs of the advanced medical manufacturing sector.
Lancing device FastClix®
- Overmolding of >1 billion needles per year,
ø: 0.3 mm x 16 mm - Multi-component and insert molding
- Fully automated, high-speed assembly with 100% in-line camera inspection
Patch pump
- Over-molding of a high-precision shaft
- High-precision micro-injection molding
- Multi-component molding
- Standard and technical plastics such as PBT, PEEK, M-ABS
Ready to realize your idea?
Our process
Product design
Industrialization
Process validation
End packaging and logistics
Weidmann Medical supports you in all steps of product development and, in parallel, creates the User Requirement Specification (URS), the Risk Management Documentation (FMEAs), and the Design History Files together with your team.
From a simple hand sketch through concept studies, product creation and design, rapid tooling and prototyping to raw material selection, cavity design, tool manufacture, and process development, we use the most modern technologies such as 3-D modeling via CAD-CAM, Moldflow Analysis, and static and dynamic calculations for part and tooling layouts.
After the User Requirement Specification (URS) is approved, Weidmann Medical develops, produces, and industrializes your product(s) according to cGMP guidelines. Our production technologies and control systems assure complete reproducibility of the entire production process.
By applying the most modern injection molding and automation technologies, we develop production processes using a combination of elastomers and non-elastomers.
All qualifications (DQ,IQ,OQ,PQ) and validation processes conform to ISO 13485 and have been certified by the DQS Agency since 2003. Weidmann Medical is audited by the FDA to the CFR820 standard and has been FDA-registered since 2013. All Cmk, Cpk-, Cp, and AQL requirements are fulfilled.
An ERP and supply chain management system enables an optimized logistics structure with both centralized and local production. Active controlling ensures continuous monitoring of the supply chain to guarantee quality and delivery reliability, while our supplier managers drive ongoing optimization.