Taiwan FDA registration 59eddbc5fab63d243d260998868a8703

"Vericom" EDTA Root Canal Preparator (Non-Sterile)

TW: "威利康" 根管擴大材 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·VERICOM CO., LTD.·Registered May 22, 2015 – May 22, 2020Cancelled
Registration details
Analysis ID
59eddbc5fab63d243d260998868a8703
License Form
Ministry of Health Medical Device Import No. 015255
Customs Code
DHA09401525501
Company information
Manufacturer
VERICOM CO., LTD.
Manufacturer Country
Korea, Republic of
Authorized Representative
HONG HOW ENTERPRISE CO.
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
May 22, 2015
Expiry Date
May 22, 2020
Cancellation Date
Jun 22, 2022
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 "Vericom" EDTA Root Canal Preparator (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 59eddbc5fab63d243d260998868a8703 and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is HONG HOW ENTERPRISE CO..

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