Taiwan FDA registration 2e70eefd50bf7c7e9ef7e0f80000f790
"BiosenWebster" Navigation Ancore Adjustable Ring Mapping Catheter
TW: “百歐森偉伯斯特”萊梭導航安可可調式環狀標測導管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Mar 24, 2015 – Mar 24, 2030ActiveRegistration details
- Analysis ID
- 2e70eefd50bf7c7e9ef7e0f80000f790
- Customs Code
- DHA05602723402
Company information
- Manufacturer
- Biosense Webster, Inc.
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Mar 24, 2015
- Expiry Date
- Mar 24, 2030
About this record
Access comprehensive regulatory information for "BiosenWebster" Navigation Ancore Adjustable Ring 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 2e70eefd50bf7c7e9ef7e0f80000f790 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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