iKAR Vita Wadent Dental Hand Instruments (Unsterilized) - Taiwan Registration d635f1fd193d60043aec553f04869656
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 d635f1fd193d60043aec553f04869656 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is TSENG LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IVOCLAR VIVADENT, INC, GEB. BRASSELER GMBH & CO KG;; 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
Oct 30, 2007
Oct 30, 2012
Apr 15, 2014
Cancellation Information
Logged out
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iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
IVOCLAR VIVADENT, INC
1046990c4d09421a9124b59fa75e5443
1
iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG
8a41eb1b1c18394bc79d3447e91e94b3
1