Taiwan FDA registration c45f50e4d053b439b582a20cad392bd5

"Jingfang" manual instruments for general surgery (unsterilized)

TW: "經方" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD.·Registered May 07, 2020 – May 07, 2025Expired
Registration details
Analysis ID
c45f50e4d053b439b582a20cad392bd5
Customs Code
DHA09600416706
Company information
Manufacturer Country
China
Authorized Representative
ROTARY TRADING CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
Input;; Chinese goods
Dates and status
Registration Date
May 07, 2020
Expiry Date
May 07, 2025
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About this record

Access comprehensive regulatory information for "Jingfang" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c45f50e4d053b439b582a20cad392bd5 and manufactured by JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD., 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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