Taiwan FDA registration 0f648eb87f3d3698af1fbaa1bae0a914

Vatek optical fiber dental light source and accessories (unsterilized)

TW: “衛得克”光纖維牙科用光源及附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD.·Registered Sep 29, 2016 – Sep 29, 2021Cancelled
Registration details
Analysis ID
0f648eb87f3d3698af1fbaa1bae0a914
Customs Code
DHA09600286701
Company information
Manufacturer Country
China
Authorized Representative
KOLN BIO-MEDICAL CO.,LTD
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.4620 Light source for optical fiber dentistry
Import Information
Chinese goods;; input
Dates and status
Registration Date
Sep 29, 2016
Expiry Date
Sep 29, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Vatek optical fiber dental light source and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0f648eb87f3d3698af1fbaa1bae0a914 and manufactured by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is KOLN BIO-MEDICAL CO.,LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GUILIN WOODPECKER MEDICAL INSTRUMENT 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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