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"Kaiwei" scraper (unsterilized) - Taiwan Registration 1cd164714db0ea70378ff63be20ed06f

Access comprehensive regulatory information for "Kaiwei" scraper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1cd164714db0ea70378ff63be20ed06f and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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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1cd164714db0ea70378ff63be20ed06f
Registration Details
Taiwan FDA Registration: 1cd164714db0ea70378ff63be20ed06f
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Device Details

"Kaiwei" scraper (unsterilized)
TW: โ€œๆ„ทๅจโ€ๅˆฎๅ™จ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

1cd164714db0ea70378ff63be20ed06f

DHA04600090503

Company Information

Product Details

It is limited to the first-level identification scope of the "Laparoscope and its Accessories for Obstetrics and Gynecology (L.1720)" of the Measures for the Classification and Grading of Medical Devices.

l Obstetrics and Gynecology

L.1720 Gynecology and gynecologic laparoscopes and their appendages

Input;; Chinese goods

Dates and Status

Apr 20, 2010

Apr 20, 2025