Taiwan FDA registration 2889a11ca8d2e43786950b30116d99c0

"Kulzer" Abrasive Device and Accessories (Non-Sterile)

TW: "古莎"研磨裝置及其附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Kulzer GmbH·Registered Oct 01, 2021 – Oct 31, 2023Expired
Registration details
Analysis ID
2889a11ca8d2e43786950b30116d99c0
License Form
Ministry of Health Medical Device Import Registration No. 018931
Customs Code
DHA08401893105
Company information
Manufacturer
Kulzer GmbH
Manufacturer Country
Germany
Authorized Representative
BENQ AB DENTCARE CORPORATION
Product details
Intended Use
Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
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
Oct 01, 2021
Expiry Date
Oct 31, 2023
Companies making similar products

Top companies providing products similar to ""Kulzer" Abrasive Device and Accessories (Non-Sterile)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Kulzer" 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 2889a11ca8d2e43786950b30116d99c0 and manufactured by Kulzer GmbH. The authorized representative in Taiwan is BENQ AB DENTCARE CORPORATION.

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

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations