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VIDA X50/R Surgical Light-Mobile Unit - Taiwan Registration 88fd11900dd35141b29842ba49c34b50

Access comprehensive regulatory information for VIDA X50/R 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 88fd11900dd35141b29842ba49c34b50 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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88fd11900dd35141b29842ba49c34b50
Registration Details
Taiwan FDA Registration: 88fd11900dd35141b29842ba49c34b50
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Device Details

VIDA X50/R Surgical Light-Mobile Unit
TW: โ€œๅบทๆบโ€็งปๅ‹•ๅผ็„กๅฝฑๆ‰‹่ก“็‡ˆ
Risk Class 2
MD
Cancelled

Registration Details

88fd11900dd35141b29842ba49c34b50

Ministry of Health Medical Device Manufacturing No. 004515

Company Information

Taiwan, Province of China

Product Details

I General and plastic surgical devices

I4580 Surgical light

Produced in Taiwan, China

Dates and Status

May 01, 2014

May 01, 2019

Jun 07, 2022

Cancellation Information

Logged out

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