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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.

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Registration Details
Taiwan FDA Registration: 8a41eb1b1c18394bc79d3447e91e94b3
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Device Details

iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
TW: โ€œ็พฉ็ฒๅ˜‰ๅ‰็“ฆ็™ป็‰นโ€็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8a41eb1b1c18394bc79d3447e91e94b3

DHA04400839606

Company Information

Liechtenstein;;Germany

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 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

Contract manufacturing;; input

Dates and Status

Dec 16, 2009

Dec 16, 2024

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