Taiwan FDA registration 40c172332348b1dad60d1b37cb72c102
“UNIMAX” Quick-Guard Wound retractor(sterile)
TW: “普威”傷口保護套(滅菌)
Taiwan·Risk Class 2·MD·Puwei International Co., Ltd. Yilan Factory·Registered Jul 21, 2017 – Jul 21, 2027ActiveRegistration details
- Analysis ID
- 40c172332348b1dad60d1b37cb72c102
- License Form
- Ministry of Health Medical Device Manufacturing No. 005886
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)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 21, 2017
- Expiry Date
- Jul 21, 2027
About this record
Access comprehensive regulatory information for “UNIMAX” Quick-Guard Wound 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 40c172332348b1dad60d1b37cb72c102 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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