Taiwan FDA registration 39e04798b867b133bd684cb7672c3cd2
“FlexDex” 8mm Needle Driver
TW: “飛達斯”機械手腕腹腔鏡持針器
Taiwan·Risk Class 2·MD·FLEXDEX INC.·Registered Jan 11, 2022 – Jan 11, 2027ActiveRegistration details
- Analysis ID
- 39e04798b867b133bd684cb7672c3cd2
- License Form
- Ministry of Health Medical Device Import No. 035178
- Customs Code
- DHA05603517801
Company information
- Manufacturer
- FLEXDEX INC.
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 11, 2022
- Expiry Date
- Jan 11, 2027
About this record
Access comprehensive regulatory information for “FlexDex” 8mm Needle Driver in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39e04798b867b133bd684cb7672c3cd2 and manufactured by FLEXDEX INC.. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., 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