Taiwan FDA registration 5912191c24019ebf584734ff7ae6bd1a
"Kentley" Yarrow chest drainage bottle
TW: "肯特利" 亞羅胸腔引流瓶
Registration details
- Analysis ID
- 5912191c24019ebf584734ff7ae6bd1a
- Customs Code
- DHA04400018607
Company information
- Manufacturer
- KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Vacuum-powered fluid absorbers are devices used to suction, remove, or sample body fluids. The device is powered by an external vacuum source.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- import
Dates and status
- Registration Date
- Jun 23, 2005
- Expiry Date
- Jun 23, 2015
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Kentley" Yarrow chest drainage bottle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5912191c24019ebf584734ff7ae6bd1a and manufactured by KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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