Taiwan FDA registration af3e44db0f465182d92e531e8dedb3ef

"Bioloren" Root Canal Post (non-sterile)

TW: "百洛" 根管中心柱釘 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BIOLOREN S.R.L.·Registered Jun 13, 2018 – Jun 13, 2023Expired
Registration details
Analysis ID
af3e44db0f465182d92e531e8dedb3ef
License Form
Ministry of Health Medical Device Import No. 019174
Customs Code
DHA09401917405
Company information
Manufacturer
BIOLOREN S.R.L.
Manufacturer Country
Italy
Authorized Representative
Zhan Sheng Biomedical 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
Jun 13, 2018
Expiry Date
Jun 13, 2023
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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 af3e44db0f465182d92e531e8dedb3ef and manufactured by BIOLOREN S.R.L.. The authorized representative in Taiwan is Zhan Sheng Biomedical 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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