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"Kindy" scope and its accessories (unsterilized) - Taiwan Registration fb3c53dd13b5f7526109542d6926824a

Access comprehensive regulatory information for "Kindy" scope and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fb3c53dd13b5f7526109542d6926824a and manufactured by TIDI PRODUCTS, LLC. The authorized representative in Taiwan is KING DAY 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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fb3c53dd13b5f7526109542d6926824a
Registration Details
Taiwan FDA Registration: fb3c53dd13b5f7526109542d6926824a
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Device Details

"Kindy" scope and its accessories (unsterilized)
TW: โ€œ้‡‘่’‚โ€ๆชขๆŸฅ้กๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fb3c53dd13b5f7526109542d6926824a

DHA04401174400

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".

I General, Plastic Surgery and Dermatology

I.1800 Inspection Scopes and Annexes

import

Dates and Status

May 24, 2012

May 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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