Taiwan FDA registration e30f80604f451041ddf7ee9419094158
“DYSIS” DYSIS Ultra Colposcope
TW: “迪席思” 電子陰道鏡成像系統
Taiwan·Risk Class 2·MD·DYSIS Medical LTD·Registered Apr 23, 2021 – Apr 23, 2026ExpiredRegistration details
- Analysis ID
- e30f80604f451041ddf7ee9419094158
- License Form
- Ministry of Health Medical Device Import No. 034510
- Customs Code
- DHA05603451001
Company information
- Manufacturer
- DYSIS Medical LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ANDERSON MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1630 Colposcopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 23, 2021
- Expiry Date
- Apr 23, 2026
About this record
Access comprehensive regulatory information for “DYSIS” DYSIS Ultra Colposcope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e30f80604f451041ddf7ee9419094158 and manufactured by DYSIS Medical LTD. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..
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