Taiwan FDA registration 40c095ef14103794651055bcf6daea59

Titanium bone plate system

TW: 鈦金屬骨板系統
Taiwan flagTaiwan·STRYKER TRAUMA-SELZACH AG·Registered Apr 03, 1998 – Apr 03, 2003Cancelled
Registration details
Analysis ID
40c095ef14103794651055bcf6daea59
Customs Code
DHA00600861702
Company information
Manufacturer Country
Switzerland
Product details
Product Type (Level 1)
0303 Artificial bone plate
Import Information
import
Dates and status
Registration Date
Apr 03, 1998
Expiry Date
Apr 03, 2003
Cancellation Date
Jul 18, 2007
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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