Taiwan FDA registration 222c1e91b621b5b7fe97bdf0bd5f39d8

"Straumann" (sterilized) accessories for healing

TW: “士卓曼”(已滅菌)癒合用配件
Taiwan flagTaiwan·Risk Class 2·INSTITUT STRAUMANN AG;; STRAUMANN MADE INC.·Registered Jan 02, 2021 – Jan 02, 2026Expired
Registration details
Analysis ID
222c1e91b621b5b7fe97bdf0bd5f39d8
Customs Code
DHA05603413909
Company information
Manufacturer Country
United States;;Switzerland
Authorized Representative
Straumann Group (Taiwan) Co. Ltd.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3630 Bolsters for intraosseous implants
Import Information
import
Dates and status
Registration Date
Jan 02, 2021
Expiry Date
Jan 02, 2026
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About this record

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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