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"KaVo" endodontic pulp canal reamer (Non-sterile) - Taiwan Registration a42e5cc0979780e45e43143efa0175fb

Access comprehensive regulatory information for "KaVo" endodontic pulp canal reamer (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 a42e5cc0979780e45e43143efa0175fb and manufactured by KALTENBACH & VOIGT GMBH. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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a42e5cc0979780e45e43143efa0175fb
Registration Details
Taiwan FDA Registration: a42e5cc0979780e45e43143efa0175fb
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Device Details

"KaVo" endodontic pulp canal reamer (Non-sterile)
TW: "ๅก็“ฆ" ๆ น็ฎก้ซ“่…”ๆ“ด้ฝ’้‘ฝ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a42e5cc0979780e45e43143efa0175fb

Ministry of Health Medical Device Import No. 014627

DHA09401462704

Company Information

Germany

Product Details

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Nov 05, 2014

Nov 05, 2019

Aug 05, 2022

Cancellation Information

Logged out

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