Taiwan FDA registration 5ab3c1909dd85863aa529eb749c7879b
"Maxell" Abdominal Inflator Accessory (Unsterilized)
TW: "麥克斯爾" 腹腔充氣機附件 (未滅菌)
Taiwan·Risk Class 1·MAXER MEDIZINTECHNIK GMBH·Registered Sep 21, 2012 – Sep 21, 2022CancelledRegistration details
- Analysis ID
- 5ab3c1909dd85863aa529eb749c7879b
- Customs Code
- DHA04401219600
Company information
- Manufacturer
- MAXER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HIGH TOP MEDICAL 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 21, 2012
- Expiry Date
- Sep 21, 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 "Maxell" Abdominal Inflator Accessory (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ab3c1909dd85863aa529eb749c7879b and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..
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