Taiwan FDA registration 76205838b8ee147af930bb930fb07afd
"McVi" Utima 2nd generation main chest dilator (unsterilized)
TW: “邁柯唯”烏提馬第二代主胸擴張器 (未滅菌)
Taiwan·Risk Class 1·MAQUET PUERTO RICO INC.·Registered Apr 21, 2006 – Apr 21, 2011CancelledRegistration details
- Analysis ID
- 76205838b8ee147af930bb930fb07afd
- Customs Code
- DHA04400415401
Company information
- Manufacturer
- MAQUET PUERTO RICO INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAYING TECHNOLOGY COMPANY
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
- Apr 21, 2006
- Expiry Date
- Apr 21, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "McVi" Utima 2nd generation main chest dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76205838b8ee147af930bb930fb07afd and manufactured by MAQUET PUERTO RICO INC.. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.
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