Taiwan FDA registration 198c988171b9efd43bf1f3904900bd36

"Qinda" belly pad (sterile/unsterilized)

TW: "勤達" 腹部墊 (滅菌/未滅菌)
Taiwan flagTaiwan·Risk Class 1·JIANGXI YA FENG MEDICAL MATERIAL CO., LTD.·Registered Jul 16, 2021 – Jul 16, 2026Expired
Registration details
Analysis ID
198c988171b9efd43bf1f3904900bd36
Customs Code
DHA09600452506
Company information
Manufacturer Country
China
Authorized Representative
TEAM POWER MEDICAL INSTRUMENT LTD.
Product details
Intended Use
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.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4450 Non-absorbable filament cloth for internal use
Import Information
Chinese goods;; QMS/QSD;; input
Dates and status
Registration Date
Jul 16, 2021
Expiry Date
Jul 16, 2026
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About this record

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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