Taiwan FDA registration b5335f85ecbfa55b7f2937baa44fdff0

VIDA Surgical Light-Mobile Unit

TW: “康源”移動式外科手術燈V系列
Taiwan flagTaiwan·Risk Class 2·MD·Kangyuan Medical Equipment Co., Ltd·Registered Dec 08, 2015 – Dec 08, 2020Cancelled
Registration details
Analysis ID
b5335f85ecbfa55b7f2937baa44fdff0
License Form
Ministry of Health Medical Device Manufacturing No. 005242
Company information
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
Dec 08, 2015
Expiry Date
Dec 08, 2020
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for VIDA Surgical Light-Mobile Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5335f85ecbfa55b7f2937baa44fdff0 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, 1 companies making similar products including Kangyuan Medical Equipment Co., Ltd, and 1 recent registrations in the same category. 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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