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"Ryder" Osterti bone graft - Taiwan Registration 374ef241e3c0623b5ddcd68636d74f4c

Access comprehensive regulatory information for "Ryder" Osterti bone graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 374ef241e3c0623b5ddcd68636d74f4c and manufactured by Wright Medical Technology, Inc.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

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.

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374ef241e3c0623b5ddcd68636d74f4c
Registration Details
Taiwan FDA Registration: 374ef241e3c0623b5ddcd68636d74f4c
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Device Details

"Ryder" Osterti bone graft
TW: โ€œ่Šๅพทโ€ๅฅงๆ–ฏ็‰นๆ้ชจ็งปๆค็‰ฉ
Risk Class 3

Registration Details

374ef241e3c0623b5ddcd68636d74f4c

DHA05603680606

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

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N.3045 Absorbable Calcium Salt Bone Cavity Filling Device

import

Dates and Status

Oct 13, 2023

Oct 13, 2028