Taiwan FDA registration 7f3224532d8b212b110d0eae99c7f42c
"Henan Camel Man" reinforced tracheal intubation
TW: “河南駝人”加強型氣管插管
Taiwan·Risk Class 2·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Dec 06, 2016 – Dec 06, 2026ActiveRegistration details
- Analysis ID
- 7f3224532d8b212b110d0eae99c7f42c
- Customs Code
- DHA09200080206
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.5730 Endotracheal tubes
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 06, 2016
- Expiry Date
- Dec 06, 2026
About this record
Access comprehensive regulatory information for "Henan Camel Man" reinforced tracheal intubation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f3224532d8b212b110d0eae99c7f42c 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