Taiwan FDA registration 9d6b14a277830f7a4487cb4d2c7246c9

"NEOLIX" Dental hand instrument (Non-Sterile)

TW: "尼歐利斯" 牙科手用器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NEOLIX SAS·Registered Jan 23, 2014 – Jan 23, 2019Cancelled
Registration details
Analysis ID
9d6b14a277830f7a4487cb4d2c7246c9
License Form
Ministry of Health Medical Device Import No. 013808
Customs Code
DHA09401380803
Company information
Manufacturer
NEOLIX SAS
Manufacturer Country
France
Authorized Representative
PRODENT CO., LTD.
Product details
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F4565 Hand instruments for dental use
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 23, 2014
Expiry Date
Jan 23, 2019
Cancellation Date
Jul 15, 2022
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 "NEOLIX" Dental hand instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d6b14a277830f7a4487cb4d2c7246c9 and manufactured by NEOLIX SAS. The authorized representative in Taiwan is PRODENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NEOLIX SAS, 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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