Taiwan FDA registration 6cbb8a7572643be0cb013fb9b7f6b697
"Kangmei" laparoscopic perfusion device attachment (sterilized)
TW: “康美”腹腔鏡灌入器附件（滅菌）
Taiwan·Risk Class 1·CONMED CORPORATION·Registered Jul 16, 2010 – Jul 16, 2020CancelledRegistration details
- Analysis ID
- 6cbb8a7572643be0cb013fb9b7f6b697
- Customs Code
- DHA04400899400
Company information
- Manufacturer
- CONMED CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1730 腹腔鏡灌入器
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 16, 2010
- Expiry Date
- Jul 16, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kangmei" laparoscopic perfusion device attachment (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6cbb8a7572643be0cb013fb9b7f6b697 and manufactured by CONMED CORPORATION. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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