Taiwan FDA registration edfbbc31917d93c6561cea489726d5df
"McVier" anesthesia breathing line (sterilization)
TW: “邁柯唯”麻醉呼吸管路 (滅菌)
Taiwan·Risk Class 1·MAQUET CRITICAL CARE AB·Registered Mar 05, 2010 – Mar 05, 2025ExpiredRegistration details
- Analysis ID
- edfbbc31917d93c6561cea489726d5df
- Customs Code
- DHA04400860400
Company information
- Manufacturer
- MAQUET CRITICAL CARE AB
- Manufacturer Country
- Sweden
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "anesthesia breathing circuit (D.5240)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5240 麻醉呼吸管路
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 05, 2010
- Expiry Date
- Mar 05, 2025
About this record
Access comprehensive regulatory information for "McVier" anesthesia breathing line (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number edfbbc31917d93c6561cea489726d5df and manufactured by MAQUET CRITICAL CARE AB. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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