iKAR Vita Wadent Dental Hand Instruments (Unsterilized) - Taiwan Registration 1046990c4d09421a9124b59fa75e5443
Access comprehensive regulatory information for iKAR Vita Wadent Dental Hand Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1046990c4d09421a9124b59fa75e5443 and manufactured by IVOCLAR VIVADENT, INC. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG, IVOCLAR VIVADENT AG, and 2 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.
Device Details
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
F Dentistry
F.4565 ็็งๆ็จๅจๆขฐ
import
Dates and Status
May 24, 2013
May 24, 2023
Mar 06, 2019
Cancellation Information
Logged out
่ช่ซ่จป้ท
iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG
8a41eb1b1c18394bc79d3447e91e94b3
1
iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
IVOCLAR VIVADENT AG
d635f1fd193d60043aec553f04869656
1