Taiwan FDA registration b372b18938c1fc8f0f66361821fb0573
"Bidi" syringe
TW: "必帝"注射筒
Registration details
- Analysis ID
- b372b18938c1fc8f0f66361821fb0573
- Customs Code
- DHA00601121301
Company information
- Manufacturer
- BECTON DICKINSON, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5860 活塞式注射筒
- Import Information
- import
Dates and status
- Registration Date
- Apr 27, 2005
- Expiry Date
- Apr 27, 2030
About this record
Access comprehensive regulatory information for "Bidi" syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b372b18938c1fc8f0f66361821fb0573 and manufactured by BECTON DICKINSON, S.A.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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