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Titanium bone plate system - Taiwan Registration 40c095ef14103794651055bcf6daea59

Access comprehensive regulatory information for Titanium bone plate system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 40c095ef14103794651055bcf6daea59 and manufactured by STRYKER TRAUMA-SELZACH AG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including STRYKER LEIBINGER GMBH & CO. KG, OSTEOSTANDARD MEDICAL DEVICE CO., LTD., and 3 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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40c095ef14103794651055bcf6daea59
Registration Details
Taiwan FDA Registration: 40c095ef14103794651055bcf6daea59
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Device Details

Titanium bone plate system
TW: ้ˆฆ้‡‘ๅฑฌ้ชจๆฟ็ณป็ตฑ
Cancelled

Registration Details

40c095ef14103794651055bcf6daea59

DHA00600861702

Company Information

Switzerland

Product Details

0303 Artificial bone plate

import

Dates and Status

Apr 03, 1998

Apr 03, 2003

Jul 18, 2007

Cancellation Information

Logged out

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