Taiwan FDA registration 51f1faf8c752df0d21e88b2ffae0757c
"Henan Camel Man" anesthesia puncture kit
TW: “河南駝人” 麻醉穿刺包
Taiwan·Risk Class 2·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Sep 21, 2018 – Sep 21, 2023ExpiredRegistration details
- Analysis ID
- 51f1faf8c752df0d21e88b2ffae0757c
- Customs Code
- DHA09200095202
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.5140 Anesthesia transfer group
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 21, 2018
- Expiry Date
- Sep 21, 2023
About this record
Access comprehensive regulatory information for "Henan Camel Man" anesthesia puncture kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51f1faf8c752df0d21e88b2ffae0757c and manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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