Taiwan FDA registration 1fc73dc3781dfbd1097d39f4e7ab3e1d
“Kitazato” IUI Catheter
TW: “北里”人工授精管
Taiwan·Risk Class 2·MD·KITAZATO Corporation·Registered Mar 04, 2016 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- 1fc73dc3781dfbd1097d39f4e7ab3e1d
- License Form
- Ministry of Health Medical Device Import No. 028249
- Customs Code
- DHA05602824904
Company information
- Manufacturer
- KITAZATO Corporation
- Manufacturer Country
- Japan
- Authorized Representative
- HONG-U SCENTIFIC CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6110 Assisted reproductive catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2016
- Expiry Date
- Mar 04, 2026
About this record
Access comprehensive regulatory information for “Kitazato” IUI Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fc73dc3781dfbd1097d39f4e7ab3e1d and manufactured by KITAZATO Corporation. The authorized representative in Taiwan is HONG-U SCENTIFIC CORP..
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