Taiwan FDA registration a29f8634b56ff5493db457c51da8909c
"DeXscope" Obstetric-gynecologic general manual instrument (Non-sterile)
TW: "帝視寰宇" 婦產科用一般手動器械 (未滅菌)
Taiwan·Risk Class 1·MD·DEX MEDICAL DEVICE CO., LTD.·Registered Sep 23, 2019 – Sep 23, 2024ExpiredRegistration details
- Analysis ID
- a29f8634b56ff5493db457c51da8909c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007966
Company information
- Manufacturer
- DEX MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DEX MEDICAL DEVICE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L4520 General manual instruments for obstetrics and gynecology
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 23, 2019
- Expiry Date
- Sep 23, 2024
About this record
Access comprehensive regulatory information for "DeXscope" Obstetric-gynecologic general manual instrument (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 a29f8634b56ff5493db457c51da8909c and manufactured by DEX MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is DEX MEDICAL DEVICE CO., LTD..
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