Taiwan FDA registration f86b0c22c77d34c739a228c0f3e90a1c
"Mai Kewei" makes up film
TW: “邁柯唯”彌補片
Taiwan·Risk Class 2·MAQUET CARDIOVASCULAR LLC·Registered Nov 23, 2010 – Nov 23, 2015CancelledRegistration details
- Analysis ID
- f86b0c22c77d34c739a228c0f3e90a1c
- Customs Code
- DHA00602172801
Company information
- Manufacturer
- MAQUET CARDIOVASCULAR LLC
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN 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.3450 血管移植彌補物
- Import Information
- import
Dates and status
- Registration Date
- Nov 23, 2010
- Expiry Date
- Nov 23, 2015
- Cancellation Date
- Jun 07, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mai Kewei" makes up film in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f86b0c22c77d34c739a228c0f3e90a1c and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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