Taiwan FDA registration 55bed855431600b4dc7f8a68130836ee
"Kedir" cardiovascular surgical instrument (unsterilized)
TW: “凱帝爾”心臟血管外科器械 (未滅菌)
Taiwan·Risk Class 1·CARDIOMEDICAL GMBH·Registered May 10, 2006 – May 10, 2011CancelledRegistration details
- Analysis ID
- 55bed855431600b4dc7f8a68130836ee
- Customs Code
- DHA04400441707
Company information
- Manufacturer
- CARDIOMEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ANSON HEALTH CARE INC.
Product details
- Intended Use
- It is limited to the scope of first-class identification of cardiovascular surgical devices (E.4500) in the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- import
Dates and status
- Registration Date
- May 10, 2006
- Expiry Date
- May 10, 2011
- Cancellation Date
- Dec 03, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kedir" cardiovascular surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55bed855431600b4dc7f8a68130836ee and manufactured by CARDIOMEDICAL GMBH. The authorized representative in Taiwan is ANSON HEALTH CARE INC..
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