iKAR Vita Wadent Dental Hand Instruments (Unsterilized) - Taiwan Registration 8a41eb1b1c18394bc79d3447e91e94b3
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 8a41eb1b1c18394bc79d3447e91e94b3 and manufactured by GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IVOCLAR VIVADENT, INC, 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
Registration Details
8a41eb1b1c18394bc79d3447e91e94b3
DHA04400839606
Product Details
Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
F Dentistry
F.4565 ็็งๆ็จๅจๆขฐ
Contract manufacturing;; input
Dates and Status
Dec 16, 2009
Dec 16, 2024
iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
IVOCLAR VIVADENT, INC
1046990c4d09421a9124b59fa75e5443
1
iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
IVOCLAR VIVADENT AG
d635f1fd193d60043aec553f04869656
1

