Taiwan FDA registration 7ed8e61e27a5e805b78d9999543dc813

"Jingfang" Manual instruments for general surgery (unsterilized)

TW: "經芳" 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 Feb 26, 2021 – Feb 26, 2026Expired
Registration details
Analysis ID
7ed8e61e27a5e805b78d9999543dc813
Customs Code
DHA09600444903
Company information
Manufacturer Country
China
Authorized Representative
LELTEK INC.
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
Chinese goods;; input
Dates and status
Registration Date
Feb 26, 2021
Expiry Date
Feb 26, 2026
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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 7ed8e61e27a5e805b78d9999543dc813 and manufactured by JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is LELTEK INC..

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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