Taiwan FDA registration 2a1199b4a46b2fa93bc44000daca1f79
"Covidien" Yarrow chest drainage bottle (sterilized)
TW: ”柯惠”亞羅胸腔引流瓶(滅菌)
Taiwan·Risk Class 1·COVIDIEN LLC;; COVIDIEN IRELAND LIMITED·Registered Jun 28, 2010 – Jun 28, 2025ExpiredRegistration details
- Analysis ID
- 2a1199b4a46b2fa93bc44000daca1f79
- Customs Code
- DHA04400894806
Company information
- Manufacturer
- COVIDIEN LLC;; COVIDIEN IRELAND LIMITED
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 28, 2010
- Expiry Date
- Jun 28, 2025
About this record
Access comprehensive regulatory information for "Covidien" Yarrow chest drainage bottle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2a1199b4a46b2fa93bc44000daca1f79 and manufactured by COVIDIEN LLC;; COVIDIEN IRELAND LIMITED. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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