Taiwan FDA registration 21a225e53350b183e33fb33e886ff857
"Biosen Webster" Ottari high-density mapping catheter
TW: “百歐森偉伯司特” 歐塔瑞高密度標測導管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Aug 30, 2022 – Aug 30, 2027ActiveRegistration details
- Analysis ID
- 21a225e53350b183e33fb33e886ff857
- Customs Code
- DHA05603577302
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 30, 2022
- Expiry Date
- Aug 30, 2027
About this record
Access comprehensive regulatory information for "Biosen Webster" Ottari 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 21a225e53350b183e33fb33e886ff857 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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