Taiwan FDA registration 4bd0b12132e534797f4f2367844dbbee
"Kitasato" embryos implanted in the catheter
TW: “北里”胚胎植入導管
Taiwan·Risk Class 2·KITAZATO Corporation·Registered Dec 27, 2011 – Dec 27, 2026ActiveRegistration details
- Analysis ID
- 4bd0b12132e534797f4f2367844dbbee
- Customs Code
- DHA00602317700
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 Obstetrics and Gynecology
- Product Type (Level 2)
- L.6110 輔助生殖導管
- Import Information
- import
Dates and status
- Registration Date
- Dec 27, 2011
- Expiry Date
- Dec 27, 2026
About this record
Access comprehensive regulatory information for "Kitasato" embryos implanted in the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4bd0b12132e534797f4f2367844dbbee and manufactured by KITAZATO Corporation. The authorized representative in Taiwan is HONG-U SCENTIFIC CORP..
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