Taiwan FDA registration efcdfe2e2ed4923c9819856c27062043
"Angib" laparoscopic surgical instruments (unsterilized)
TW: “安吉必”腹腔鏡手術器械(未滅菌)
Taiwan·Risk Class 1·MGB ENDOSCOPIC DEVICES GMBH BERLIN·Registered Apr 17, 2009 – Apr 17, 2014CancelledRegistration details
- Analysis ID
- efcdfe2e2ed4923c9819856c27062043
- Customs Code
- DHA04400764802
Company information
- Manufacturer
- MGB ENDOSCOPIC DEVICES GMBH BERLIN
- Manufacturer Country
- Germany
- Authorized Representative
- HURRAYBIO CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Laparoscopy and Its Accessories for Obstetrics and Gynecology (L.1720)".
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1720 Gynecology and gynecologic laparoscopes and their appendages
- Import Information
- import
Dates and status
- Registration Date
- Apr 17, 2009
- Expiry Date
- Apr 17, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Angib" laparoscopic surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number efcdfe2e2ed4923c9819856c27062043 and manufactured by MGB ENDOSCOPIC DEVICES GMBH BERLIN. The authorized representative in Taiwan is HURRAYBIO CO., LTD..
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