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"Straumann" (sterilized) accessories for healing - Taiwan Registration 222c1e91b621b5b7fe97bdf0bd5f39d8

Access comprehensive regulatory information for "Straumann" (sterilized) accessories for healing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 222c1e91b621b5b7fe97bdf0bd5f39d8 and manufactured by INSTITUT STRAUMANN AG;; STRAUMANN MADE INC.. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Straumann Villeret SA;; Institut Straumann AG, 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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222c1e91b621b5b7fe97bdf0bd5f39d8
Registration Details
Taiwan FDA Registration: 222c1e91b621b5b7fe97bdf0bd5f39d8
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Device Details

"Straumann" (sterilized) accessories for healing
TW: โ€œๅฃซๅ“ๆ›ผโ€(ๅทฒๆป…่Œ)็™’ๅˆ็”จ้…ไปถ
Risk Class 2

Registration Details

222c1e91b621b5b7fe97bdf0bd5f39d8

DHA05603413909

Company Information

United States;;Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

F Dentistry

F.3630 Bolsters for intraosseous implants

import

Dates and Status

Jan 02, 2021

Jan 02, 2026

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