Taiwan FDA registration 279eda0783ffb2f68a746dd4c24f4659
"Bonshi" excision mirror
TW: “邦士”切除鏡
Taiwan·Risk Class 2·Jiangsu Bonss Medical Technology Co., Ltd.·Registered Jan 03, 2024 – Jan 03, 2029ActiveRegistration details
- Analysis ID
- 279eda0783ffb2f68a746dd4c24f4659
- Customs Code
- DHA09200153300
Company information
- Manufacturer
- Jiangsu Bonss Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 03, 2024
- Expiry Date
- Jan 03, 2029
About this record
Access comprehensive regulatory information for "Bonshi" excision mirror in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 279eda0783ffb2f68a746dd4c24f4659 and manufactured by Jiangsu Bonss Medical Technology Co., Ltd.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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