Taiwan FDA registration bb608d57f2fcadc1247e71567a3033f3
“Merit” Brighton Bipolar Coagulation Probe
TW: “美瑞特”拜博凝血探頭
Taiwan·Risk Class 2·MD·Merit Medical Systems, Inc.·Registered Aug 19, 2013 – Aug 19, 2023ExpiredRegistration details
- Analysis ID
- bb608d57f2fcadc1247e71567a3033f3
- License Form
- Ministry of Health Medical Device Import No. 025377
- Customs Code
- DHA05602537701
Company information
- Manufacturer
- Merit Medical Systems, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Merit Medical Asia Company Limited Taiwan Branch (Hong Kong)
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)
- H4300 Electrocutors for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 19, 2013
- Expiry Date
- Aug 19, 2023
About this record
Access comprehensive regulatory information for “Merit” Brighton Bipolar Coagulation Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb608d57f2fcadc1247e71567a3033f3 and manufactured by Merit Medical Systems, Inc.. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).
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