Taiwan FDA registration 81a5042ef81132ee191fe34c77e6a927
"Biodex" Syringe and Vial Shields (Non-Sterile)
TW: "貝奧德士" 注射器及容器防護屏蔽 (未滅菌)
Registration details
- Analysis ID
- 81a5042ef81132ee191fe34c77e6a927
- License Form
- Ministry of Health Medical Device Import No. 015644
- Customs Code
- DHA09401564409
Company information
- Manufacturer
- BIODEX MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GLOBAL MEDICAL SOLUTIONS TAIWAN, LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Personal Protective Shield (P.6500)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P6500 Personal Shield
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 03, 2015
- Expiry Date
- Sep 03, 2025
About this record
Access comprehensive regulatory information for "Biodex" Syringe and Vial Shields (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 81a5042ef81132ee191fe34c77e6a927 and manufactured by BIODEX MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is GLOBAL MEDICAL SOLUTIONS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices