Taiwan FDA registration 64e79a81f4589df86bf454926499a7d4
"Henan camel man" double-lumen bronchial atresia catheter
TW: “河南駝人”雙腔支氣管閉鎖導管
Taiwan·Risk Class 2·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Dec 22, 2016 – Dec 22, 2026ActiveRegistration details
- Analysis ID
- 64e79a81f4589df86bf454926499a7d4
- Customs Code
- DHA09200080502
Company information
- Manufacturer
- HENAN TUOREN MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5740 Gas pipe/bronchi divergence gas line
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 22, 2016
- Expiry Date
- Dec 22, 2026
About this record
Access comprehensive regulatory information for "Henan camel man" double-lumen bronchial atresia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 64e79a81f4589df86bf454926499a7d4 and manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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