Taiwan FDA registration 70e733b16db5a60375698044c1d7ccaf
"Xingchang" inner Lou tubular wing needle group
TW: “杏昌”內婁管翼狀針組
Taiwan·Risk Class 2·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered May 09, 2012 – May 09, 2027ActiveRegistration details
- Analysis ID
- 70e733b16db5a60375698044c1d7ccaf
- Customs Code
- DHA04200044005
Company information
- Manufacturer
- BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- May 09, 2012
- Expiry Date
- May 09, 2027
About this record
Access comprehensive regulatory information for "Xingchang" inner Lou tubular wing needle group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70e733b16db5a60375698044c1d7ccaf and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is HI-CLEARANCE INC..
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