Taiwan FDA registration 052da04a89892a5cee5ea77e8b4b2474

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 Apr 27, 2010 – Apr 27, 2015Cancelled
Registration details
Analysis ID
052da04a89892a5cee5ea77e8b4b2474
Customs Code
DHA04600091404
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
Apr 27, 2010
Expiry Date
Apr 27, 2015
Cancellation Date
Nov 09, 2015
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 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 052da04a89892a5cee5ea77e8b4b2474 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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