"BOTISS" Endosseous dental implant accessories (Non-Sterile) - Taiwan Registration 86adbd5c1d2a87e8057054387c0c5b47
Access comprehensive regulatory information for "BOTISS" Endosseous dental implant accessories (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 86adbd5c1d2a87e8057054387c0c5b47 and manufactured by BOTISS BIOMATERIALS GMBH. The authorized representative in Taiwan is Jintaiyang Enterprise Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BOTISS BIOMATERIALS GMBH, and 1 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
86adbd5c1d2a87e8057054387c0c5b47
Ministry of Health Medical Device Import No. 017224
DHA09401722400
Product Details
Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
F Dental devices
F3980 Dental Intraosseous Implant Attachment
Imported from abroad
Dates and Status
Nov 29, 2016
Nov 29, 2021

