Taiwan FDA registration 91722aca14934cbeffb3ef0146640b8d
"Expand the Fit" Genie drug delivery balloon catheter
TW: “擴適達”精靈藥物輸送氣球導管
Taiwan·Risk Class 2·ACROSTAK (SCHWEIZ) AG·Registered Dec 11, 2012 – Dec 11, 2022CancelledRegistration details
- Analysis ID
- 91722aca14934cbeffb3ef0146640b8d
- Customs Code
- DHA00602424904
Company information
- Manufacturer
- ACROSTAK (SCHWEIZ) AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- WATTCAN INSTRUMENTS CO., 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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Dec 11, 2012
- Expiry Date
- Dec 11, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Expand the Fit" Genie drug delivery balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91722aca14934cbeffb3ef0146640b8d and manufactured by ACROSTAK (SCHWEIZ) AG. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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