Taiwan FDA registration e21ccf3c77116acd619e4649d689a62c
Laparoscopic attachment for obstetrics and gynecology "Arkmen" (unsterilized)
TW: “亞克門”婦產科用腹腔鏡附件（未滅菌）
Taiwan·Risk Class 1·ACKERMANN INSTRUMENTE GMBH·Registered Dec 14, 2007 – Dec 14, 2022CancelledRegistration details
- Analysis ID
- e21ccf3c77116acd619e4649d689a62c
- Customs Code
- DHA04400639000
Company information
- Manufacturer
- ACKERMANN INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS 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
- Dec 14, 2007
- Expiry Date
- Dec 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 Laparoscopic attachment for obstetrics and gynecology "Arkmen" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e21ccf3c77116acd619e4649d689a62c and manufactured by ACKERMANN INSTRUMENTE GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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