Taiwan FDA registration 375cb9659b0710cdb31d50b83d937d45

"Kindy" medical gauze (unsterilized)

TW: "金蒂"醫用紗布(未滅菌)
Taiwan flagTaiwan·Risk Class 1·HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.·Registered Nov 27, 2012 – Nov 27, 2022Cancelled
Registration details
Analysis ID
375cb9659b0710cdb31d50b83d937d45
Customs Code
DHA04600179501
Company information
Manufacturer Country
China
Authorized Representative
KING DAY CO., LTD.
Product details
Intended Use
Limited to the first level of identification scope of "external use of non-absorbent gauze or sponge balls (I.4014)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4014 Non-absorbent cloth or sea balls are used externally
Import Information
Chinese goods;; input
Dates and status
Registration Date
Nov 27, 2012
Expiry Date
Nov 27, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Kindy" medical gauze (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 375cb9659b0710cdb31d50b83d937d45 and manufactured by HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is KING DAY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including XIANTAO JIALING MEDICAL PRODUCTS 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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