Taiwan FDA registration 68a544d4bc7a4485a47c27f247f6faea
"Biosen Webster" ultrasound catheter for diagnosis
TW: “百歐森偉伯司特” 診斷用超音波導管
Taiwan·Risk Class 2·Siemens Healthineers Ltd.;; Siemens Medical Solutions USA, Inc.·Registered Oct 13, 2023 – Oct 13, 2028ActiveRegistration details
- Analysis ID
- 68a544d4bc7a4485a47c27f247f6faea
- Customs Code
- DHA05603662502
Company information
- Manufacturer Country
- Korea, Republic of;;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.1200 診斷用血管內導管
- Import Information
- import
Dates and status
- Registration Date
- Oct 13, 2023
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for "Biosen Webster" ultrasound catheter for diagnosis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68a544d4bc7a4485a47c27f247f6faea and manufactured by Siemens Healthineers Ltd.;; Siemens Medical Solutions USA, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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