"Kehao-style" Peritai Esp implant system - Taiwan Registration d7cb2d4bc7e7e3fb4c80b82eb6daccd5
Access comprehensive regulatory information for "Kehao-style" Peritai Esp implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d7cb2d4bc7e7e3fb4c80b82eb6daccd5 and manufactured by CLINICAL HOUSE EUROPE GMBH. The authorized representative in Taiwan is ARCHER MEDICAL TRADING CORP..
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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
F Dentistry
F.3640 Bone Implants
import
Dates and Status
May 05, 2011
Nov 09, 2015
Apr 25, 2018
Cancellation Information
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