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"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.

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86adbd5c1d2a87e8057054387c0c5b47
Registration Details
Taiwan FDA Registration: 86adbd5c1d2a87e8057054387c0c5b47
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Device Details

"BOTISS" Endosseous dental implant accessories (Non-Sterile)
TW: "ๆณขๆๆ–ฏ" ็‰™้ฝ’้ชจๅ…งๆคๅ…ฅ็‰ฉ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

86adbd5c1d2a87e8057054387c0c5b47

Ministry of Health Medical Device Import No. 017224

DHA09401722400

Company Information

Germany

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

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