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"Qinda" belly pad (sterile/unsterilized) - Taiwan Registration 198c988171b9efd43bf1f3904900bd36

Access comprehensive regulatory information for "Qinda" belly pad (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 198c988171b9efd43bf1f3904900bd36 and manufactured by JIANGXI YA FENG MEDICAL MATERIAL CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOSPITECH MANUFACTURING SERVICES SDN BHD, 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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198c988171b9efd43bf1f3904900bd36
Registration Details
Taiwan FDA Registration: 198c988171b9efd43bf1f3904900bd36
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Device Details

"Qinda" belly pad (sterile/unsterilized)
TW: "ๅ‹ค้”" ่…น้ƒจๅขŠ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

198c988171b9efd43bf1f3904900bd36

DHA09600452506

Company Information

Product Details

It is limited to the first level of identification of the "non-absorbable gauze for internal use (I.4450)" of the Administrative Measures for the Classification and Grading of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4450 Non-absorbable filament cloth for internal use

Chinese goods;; QMS/QSD;; input

Dates and Status

Jul 16, 2021

Jul 16, 2026

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