Taiwan FDA registration 62c9b5af7b11af383a2335df0c5707b1
"Rudolph" laparoscopic perfusion device (unsterilized)
TW: “魯道夫” 腹腔鏡灌入器 (未滅菌)
Taiwan·Risk Class 1·RUDOLF MEDICAL GMBH + CO. KG·Registered Sep 14, 2012 – Sep 14, 2022CancelledRegistration details
- Analysis ID
- 62c9b5af7b11af383a2335df0c5707b1
- Customs Code
- DHA04401216107
Company information
- Manufacturer
- RUDOLF MEDICAL GMBH + CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- EVERMED INTERNATIONAL 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
- import
Dates and status
- Registration Date
- Sep 14, 2012
- Expiry Date
- Sep 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rudolph" laparoscopic perfusion device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 62c9b5af7b11af383a2335df0c5707b1 and manufactured by RUDOLF MEDICAL GMBH + CO. KG. The authorized representative in Taiwan is EVERMED INTERNATIONAL CO., LTD..
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