Taiwan FDA registration e73c3960949a9b3d8afe0bb660cd70b8
"Visionsense" Gynecologic laparoscope accessories (Non-Sterile)
TW: "微晰見視" 婦產科用腹腔鏡附件 (未滅菌)
Taiwan·Risk Class 1·MD·VISIONSENSE LTD.·Registered Aug 21, 2015 – Aug 21, 2020CancelledRegistration details
- Analysis ID
- e73c3960949a9b3d8afe0bb660cd70b8
- License Form
- Ministry of Health Medical Device Import No. 015599
- Customs Code
- DHA09401559904
Company information
- Manufacturer
- VISIONSENSE LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1720 Laparoscopy for obstetrics and gynecology and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 21, 2015
- Expiry Date
- Aug 21, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Visionsense" Gynecologic laparoscope accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e73c3960949a9b3d8afe0bb660cd70b8 and manufactured by VISIONSENSE LTD.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices