Taiwan FDA registration 92f2ce06017f362bdf2b934c4f24245d
"Ji Qi" El Fidalip laparoscopic perfusion device and its accessories
TW: "吉銤"艾爾菲達力普腹腔鏡灌入器及其附件
Taiwan·Risk Class 2·GIMMI GMBH.·Registered Sep 04, 2006 – Sep 04, 2016CancelledRegistration details
- Analysis ID
- 92f2ce06017f362bdf2b934c4f24245d
- Customs Code
- DHA00601707302
Company information
- Manufacturer
- GIMMI GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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 04, 2006
- Expiry Date
- Sep 04, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ji Qi" El Fidalip laparoscopic perfusion device and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92f2ce06017f362bdf2b934c4f24245d and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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