Taiwan FDA registration b75c6552ccaf2e68d6a7a7d69a0c15b5
“Henan Tuoren” Endotracheal Tube
TW: “河南駝人” 氣管內管
Taiwan·Risk Class 2·MD·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Dec 11, 2018 – Dec 11, 2028ActiveRegistration details
- Analysis ID
- b75c6552ccaf2e68d6a7a7d69a0c15b5
- License Form
- Ministry of Health Medical Device Land Transport No. 000964
- Customs Code
- DHA09200096406
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 Devices for anesthesiology
- Product Type (Level 2)
- D5730 Endotracheal tube
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Dec 11, 2018
- Expiry Date
- Dec 11, 2028
About this record
Access comprehensive regulatory information for “Henan Tuoren” Endotracheal Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b75c6552ccaf2e68d6a7a7d69a0c15b5 and manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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