Taiwan FDA registration dda360c1b576ccbaf7eccce0f2234c4e

"Bioloren" Root Canal Post (Non-Sterile)

TW: "拜羅倫" 根管中心柱釘 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BIOLOREN S.R.L.·Registered Mar 08, 2017 – Mar 08, 2022Expired
Registration details
Analysis ID
dda360c1b576ccbaf7eccce0f2234c4e
License Form
Ministry of Health Medical Device Import No. 017571
Customs Code
DHA09401757105
Company information
Manufacturer
BIOLOREN S.R.L.
Manufacturer Country
Italy
Authorized Representative
HONG SHIN DENTAL MATERIAL CO., LTD
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3810 tube center column nail
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 08, 2017
Expiry Date
Mar 08, 2022
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About this record

Access comprehensive regulatory information for "Bioloren" Root Canal Post (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 dda360c1b576ccbaf7eccce0f2234c4e and manufactured by BIOLOREN S.R.L.. The authorized representative in Taiwan is HONG SHIN DENTAL MATERIAL CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOLOREN S.R.L., 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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