Taiwan FDA registration 0f37583f3ffa2f96694ac05ad32dc5ed
“UNIMAX” Single Port Access System (Sterile)
TW: “普威”單孔多器械手術通路系統(滅菌)
Taiwan·Risk Class 2·MD·Puwei International Co., Ltd. Yilan Factory·Registered Sep 05, 2017 – Sep 05, 2027ActiveRegistration details
- Analysis ID
- 0f37583f3ffa2f96694ac05ad32dc5ed
- License Form
- Ministry of Health Medical Device Manufacturing No. 005901
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
- Sep 05, 2017
- Expiry Date
- Sep 05, 2027
About this record
Access comprehensive regulatory information for “UNIMAX” Single Port Access System (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f37583f3ffa2f96694ac05ad32dc5ed and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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