Search F2 TechNotes
Categories
- ASCA Program
- ATEX Directive 2014/34/EU
- Batteries
- CE marking
- Consulting
- EMC Directive 2014/30/EU
- EMC Testing
- EN 60601-1
- EU Battery Regulation (EU)2023/152
- EVs
- FCC
- FDA
- Field Label
- General Product Safety Directive 2001/95/EC
- General Product Safety Regulation (EU) 2023/988
- GPSR
- GPSR (EU)2023/988
- IEC 60601-1-9
- International Testing
- IP Testing
- Lasers
- Listing
- Low Voltage Directive 2014/35/EU
- Machinery Directive 2006/42/EC
- Machinery Regulation (EU)2023/1230
- Medical Devices Regulation (EU)2017/745
- PPE Regulation (EU) 2016/425
- Pressure Equipment Directive 2014/68/EU
- Product Testing
- Prop 65
- R&TTE Directive 1999/5/EC
- Radio Equipment Directive 2014/53/EU
- REACH
- RoHS Directive 2011/65/EU
- SPE-1000
- UKCA
- UL 4200A
- UL 60335-1
- UL 61010-1
- UL 62368-1
- UL 94
- US Field Label
-
Recent Posts
February 2024 M T W T F S S 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29
Daily Archives: February 29, 2024
FDA Advises Medical Device Manufacturers to be Vigilant and Validate Data
The U.S. Food and Drug Administration recently sent out an Open Letter to Industry to remind manufacturers of medical devices that they should always be vigilant in verifying the accuracy of third party testing data that they are using for … Continue reading
Posted in FCC, FDA, Product Testing
Comments Off on FDA Advises Medical Device Manufacturers to be Vigilant and Validate Data