Taiwan FDA registration 9258d13b4dde70b2347b8cb72db30469
“TMP” PTA Balloon Catheter
TW: “東海”氣球擴張導管
Taiwan·Risk Class 2·MD·Tokai Medical Products, Inc., Toki Factory·Registered Jun 13, 2016 – Jun 13, 2026ExpiredRegistration details
- Analysis ID
- 9258d13b4dde70b2347b8cb72db30469
- License Form
- Ministry of Health Medical Device Import No. 028603
- Customs Code
- DHA05602860309
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
- Jun 13, 2016
- Expiry Date
- Jun 13, 2026
About this record
Access comprehensive regulatory information for “TMP” PTA Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9258d13b4dde70b2347b8cb72db30469 and manufactured by Tokai Medical Products, Inc., Toki Factory. The authorized representative in Taiwan is HI-CLEARANCE INC..
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