Taiwan FDA registration cdb32d878744af1c98c49ebd3d6e0802
“UNIMAX” Uterine Manipulator/Retractor (sterile)
TW: “普威”子宮灌注操縱器(滅菌)
Taiwan·Risk Class 2·MD·Puwei International Co., Ltd. Yilan Factory·Registered Jun 09, 2017 – Jun 09, 2027ActiveRegistration details
- Analysis ID
- cdb32d878744af1c98c49ebd3d6e0802
- License Form
- Ministry of Health Medical Device Manufacturing No. 005777
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
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)
- L4530 Manual instruments for obstetrics and gynecology
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 09, 2017
- Expiry Date
- Jun 09, 2027
About this record
Access comprehensive regulatory information for “UNIMAX” Uterine Manipulator/Retractor (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdb32d878744af1c98c49ebd3d6e0802 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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