Taiwan FDA registration fa8a5806c7eb5e565304514e68617a4a
"Biosen Webster" Mobicar atrial diaphragmatic puncture needle
TW: “百歐森偉伯司特”摩比卡斯心房中膈穿刺針
Taiwan·Risk Class 2·GREATBATCH MEDICAL INC·Registered May 17, 2013 – May 17, 2018CancelledRegistration details
- Analysis ID
- fa8a5806c7eb5e565304514e68617a4a
- Customs Code
- DHA00602489601
Company information
- Manufacturer
- GREATBATCH MEDICAL INC
- Manufacturer Country
- 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.1390 Casing needle
- Import Information
- import
Dates and status
- Registration Date
- May 17, 2013
- Expiry Date
- May 17, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Biosen Webster" Mobicar atrial diaphragmatic puncture needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa8a5806c7eb5e565304514e68617a4a and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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