Taiwan FDA registration c097d88f7f977843dfad8fe4379295fc
"Kaijie" cervical kit
TW: “凱杰”子宮頸採檢套組
Taiwan·Risk Class 2·QIAGEN·Registered Nov 29, 2012 – Nov 29, 2027ActiveRegistration details
- Analysis ID
- c097d88f7f977843dfad8fe4379295fc
- Customs Code
- DHA00602423802
Company information
- Manufacturer
- QIAGEN
- Manufacturer Country
- United States
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
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.4530 婦產科專用手動器械
- Import Information
- import
Dates and status
- Registration Date
- Nov 29, 2012
- Expiry Date
- Nov 29, 2027
About this record
Access comprehensive regulatory information for "Kaijie" cervical kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c097d88f7f977843dfad8fe4379295fc and manufactured by QIAGEN. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
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