Taiwan FDA registration d99d428beac5f55474a0ddf02fda50c3
"Bayerson" Geheer quickly withdraws the coronary artery stent system
TW: “拜爾生”格希爾快速抽換冠狀動脈支架系統
Taiwan·Risk Class 3·BIOSENSORS INTERNATIONAL PTE. LTD.·Registered Feb 15, 2008 – Feb 15, 2013CancelledRegistration details
- Analysis ID
- d99d428beac5f55474a0ddf02fda50c3
- Customs Code
- DHA00601859600
Company information
- Manufacturer
- BIOSENSORS INTERNATIONAL PTE. LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- KINGDOM EAST ENTERPRISE 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.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Feb 15, 2008
- Expiry Date
- Feb 15, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayerson" Geheer quickly withdraws the coronary artery stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d99d428beac5f55474a0ddf02fda50c3 and manufactured by BIOSENSORS INTERNATIONAL PTE. LTD.. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..
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