Taiwan FDA registration f0ed451c70b2a849abd3af11e0a2a4a3
"McVi" cardiovascular surgery instrument (sterilization)
TW: “邁柯唯”心臟血管外科器械 (滅菌）
Taiwan·Risk Class 1·MAQUET CARDIOVASCULAR LLC·Registered Mar 10, 2009 – Mar 10, 2024ExpiredRegistration details
- Analysis ID
- f0ed451c70b2a849abd3af11e0a2a4a3
- Customs Code
- DHA04400754301
Company information
- Manufacturer
- MAQUET CARDIOVASCULAR LLC
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 10, 2009
- Expiry Date
- Mar 10, 2024
About this record
Access comprehensive regulatory information for "McVi" cardiovascular surgery instrument (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f0ed451c70b2a849abd3af11e0a2a4a3 and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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