Taiwan FDA registration 034955c5dc1c9f22c69a8e0d19f0f83c
Wei Gene Vaginal Lavator (Unsterilized)
TW: 薇基因 陰道灌洗器 (未滅菌)
Taiwan·Risk Class 1·JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Jun 21, 2019 – Jun 21, 2029ActiveRegistration details
- Analysis ID
- 034955c5dc1c9f22c69a8e0d19f0f83c
Company information
- Manufacturer
- JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Leye Biochemical Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "Therapeutic Vaginal Lavage Device (L.5900)".
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.5900 治療用陰道灌洗器
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jun 21, 2019
- Expiry Date
- Jun 21, 2029
About this record
Access comprehensive regulatory information for Wei Gene Vaginal Lavator (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 034955c5dc1c9f22c69a8e0d19f0f83c and manufactured by JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Leye Biochemical Technology Co., Ltd.
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