Taiwan FDA registration 989d3de3a83d255e791960ce3e174848
VIDA LED Examination Light-X5 Series
TW: “康源”醫學檢查燈X5系列
Taiwan·Risk Class 2·MD·Kangyuan Medical Equipment Co., Ltd·Registered Nov 11, 2014 – Nov 11, 2019CancelledRegistration details
- Analysis ID
- 989d3de3a83d255e791960ce3e174848
- License Form
- Ministry of Health Medical Device Manufacturing No. 004696
Company information
- Manufacturer
- Kangyuan Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kangyuan Medical Equipment Co., Ltd
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4580 Surgical light
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 11, 2014
- Expiry Date
- Nov 11, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for VIDA LED Examination Light-X5 Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 989d3de3a83d255e791960ce3e174848 and manufactured by Kangyuan Medical Equipment Co., Ltd. The authorized representative in Taiwan is Kangyuan Medical Equipment 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.
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