General questions
Does the Accu-Chek Safe-T-Pro Uno lancing device meet legal requirements?
Roche Diabetes Care, as a manufacturer of medical devices, certified to European standards, complies with all applicable European directives. The lancing device is CE (Conformité Européene) labeled, which means that the product meets the safety and normative requirements of those European directives. The European regulations are valid and recognized under mutual recognition agreements with many countries, including Canada, LATAM, APAC and Japan. The lancing device also complies with laws such as the US Needlestick Safety and Prevention Act, the TRBA 250 (Germany) or the NR 32 (Brazil) and others.
Other categories
Check other FAQ categories by clicking on the below category names.
- Accuracy
- Test strips
- Getting started
- Launch Dates
- Specifications
- Meter Settings
- General Use
- Data
- Connectivity
- Chemistry
- Blood Sample
- Strip Container
- Control - Linearity Solutions
- Interferences - Limitations
- Digital Solution Compatibility
- Intended Use, Documents for Registration Purposes
- Product Materials, Bill of Materials
- Hygiene, Sterility, Lancet Reuse, Disposal of Used Consumables
- Needle, Lancet
- Lancing Depth, Depth Settings
- Alternative Site Testing (AST)
- Clixmotion Technology
- 1-Click Lancing
- Lancing - Steps, Helpful Information
- Patents, Generics, Counterfeits