Taiwan FDA registration 19d8d19132e38bf59844f9c196e23402
"Kidme" germ cell culture reagent
TW: “吉德美”生殖細胞培養試劑
Taiwan·Risk Class 2·GYNEMED GmbH & Co. KG·Registered Jun 14, 2019 – Jun 14, 2029ActiveRegistration details
- Analysis ID
- 19d8d19132e38bf59844f9c196e23402
- Customs Code
- DHA05603263307
Company information
- Manufacturer
- GYNEMED GmbH & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- MING-MEI TECHNOLOGY CO., LTD.
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.6180 Vectors and supplements for reproductive use
- Import Information
- import
Dates and status
- Registration Date
- Jun 14, 2019
- Expiry Date
- Jun 14, 2029
About this record
Access comprehensive regulatory information for "Kidme" germ cell culture reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19d8d19132e38bf59844f9c196e23402 and manufactured by GYNEMED GmbH & Co. KG. The authorized representative in Taiwan is MING-MEI TECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices