Taiwan FDA registration 8ff497c7dd38045bedbdf2ae77d9ed93
"FlexDex" Gynecologic laparoscope and accessories (Sterile)
TW: "飛達斯" 婦產科用腹腔鏡及其附件(滅菌)
Taiwan·Risk Class 1·MD·FLEXDEX INC.·Registered Feb 10, 2020 – Feb 10, 2025ExpiredRegistration details
- Analysis ID
- 8ff497c7dd38045bedbdf2ae77d9ed93
- License Form
- Ministry of Health Medical Device Import No. 021242
- Customs Code
- DHA09402124201
Company information
- Manufacturer
- FLEXDEX INC.
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS 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 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
- Feb 10, 2020
- Expiry Date
- Feb 10, 2025
About this record
Access comprehensive regulatory information for "FlexDex" Gynecologic laparoscope and accessories (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ff497c7dd38045bedbdf2ae77d9ed93 and manufactured by FLEXDEX INC.. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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