All TPP products are manufactured from fully synthetic raw materials and contain no components of animal origin.
The materials used meet recognized standards for medical and laboratory applications, including:
- Compliance with USP Class VI biocompatibility requirements
- Use of medical-grade raw materials
TPP products are classified according to applicable European medical device regulations. The former Directive 93/42/EEC (MDD) has been replaced by the current Regulation (EU) 2017/745 (MDR), which now defines the regulatory framework.
TSE/BSE compliance
All TPP products are:
- animal origin-free
- free from TSE/BSE (Transmissible Spongiform Encephalopathy / Bovine Spongiform Encephalopathy)
- manufactured without the use of specified risk materials (SRM) in accordance with relevant EU requirements
User-relevant summary
- No risk from animal-derived contamination
- Suitable for sensitive applications in cell culture, diagnostics, and research
- Aligned with current regulatory and biocompatibility standards