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"Kaiwei" introduction sleeve and its accessories (unsterilized) - Taiwan Registration 0bd25f036a791ab23085f25639579b55

Access comprehensive regulatory information for "Kaiwei" introduction sleeve 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 0bd25f036a791ab23085f25639579b55 and manufactured by KAI WEI (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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0bd25f036a791ab23085f25639579b55
Registration Details
Taiwan FDA Registration: 0bd25f036a791ab23085f25639579b55
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Device Details

"Kaiwei" introduction sleeve and its accessories (unsterilized)
TW: โ€œๆ„ทๅจโ€ๅฐŽๅ…ฅๅฅ—็ฎกๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0bd25f036a791ab23085f25639579b55

DHA04600025302

Company Information

Product Details

Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Input;; Chinese goods

Dates and Status

May 25, 2006

May 25, 2026