Taiwan FDA registration 8276154aec8d945769f53b871283d765
“Ming-mei” Cryotech Vitrification and Warming Kits
TW: “明美”卵與胚胎保存系統
Taiwan·Risk Class 2·MD·REPROLIFE Inc.·Registered Oct 29, 2018 – Oct 29, 2028ActiveRegistration details
- Analysis ID
- 8276154aec8d945769f53b871283d765
- License Form
- Ministry of Health Medical Device Import No. 031835
- Customs Code
- DHA05603183501
Company information
- Manufacturer
- REPROLIFE Inc.
- Manufacturer Country
- Japan
- 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 Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6180 Reproductive vehicles and supplements
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 29, 2018
- Expiry Date
- Oct 29, 2028
About this record
Access comprehensive regulatory information for “Ming-mei” Cryotech Vitrification and Warming Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8276154aec8d945769f53b871283d765 and manufactured by REPROLIFE Inc.. The authorized representative in Taiwan is MING-MEI TECHNOLOGY CO., LTD..
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