Taiwan FDA registration 9c0d1a734183649b0e7952e80b834334

“EST” Abrasive device and accessories (Non-Sterile)

TW: “憶生堂” 研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Ivoclar Vivadent Manufacturing GmbH·Registered Jul 15, 2019 – Jul 15, 2024Cancelled
Registration details
Analysis ID
9c0d1a734183649b0e7952e80b834334
License Form
Ministry of Health Medical Device Import No. 020650
Customs Code
DHA09402065001
Company information
Manufacturer Country
Austria
Authorized Representative
E.S.T. BIOTECH INC.
Product details
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6010 Grinding device and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 15, 2019
Expiry Date
Jul 15, 2024
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for “EST” Abrasive device and accessories (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 9c0d1a734183649b0e7952e80b834334 and manufactured by Ivoclar Vivadent Manufacturing GmbH. The authorized representative in Taiwan is E.S.T. BIOTECH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Ivoclar Vivadent Manufacturing GmbH, 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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