Taiwan FDA registration ace3f2b5f412c7760386d51ecc38824c
"Biosen Webster" Opryl high-density mapping catheter
TW: “百歐森偉伯斯特” 歐普瑞爾高密度標測導管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Aug 21, 2023 – Aug 21, 2028ActiveRegistration details
- Analysis ID
- ace3f2b5f412c7760386d51ecc38824c
- Customs Code
- DHA05603658302
Company information
- Manufacturer
- Biosense Webster, Inc.
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1220 電極記錄導管或電極記錄探頭
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2023
- Expiry Date
- Aug 21, 2028
About this record
Access comprehensive regulatory information for "Biosen Webster" Opryl high-density mapping catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ace3f2b5f412c7760386d51ecc38824c and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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