Taiwan FDA registration f0eb5ac0931451302795b668ef72c23f
“TMP” Rescue Balloon Occlusion Catheter
TW: “東海”銳思克閉塞球囊導管
Taiwan·Risk Class 2·MD·Tokai Medical Products, Inc., Toki Factory·Registered Jan 23, 2019 – Jan 23, 2024ExpiredRegistration details
- Analysis ID
- f0eb5ac0931451302795b668ef72c23f
- License Form
- Ministry of Health Medical Device Import No. 032086
- Customs Code
- DHA05603208604
Company information
- Manufacturer
- Tokai Medical Products, Inc., Toki Factory
- Manufacturer Country
- Japan
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 23, 2019
- Expiry Date
- Jan 23, 2024
About this record
Access comprehensive regulatory information for “TMP” Rescue Balloon Occlusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0eb5ac0931451302795b668ef72c23f and manufactured by Tokai Medical Products, Inc., Toki Factory. The authorized representative in Taiwan is HI-CLEARANCE INC..
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