Taiwan FDA registration a04e30fdecb8c3c470394dc73f320856

"Stryker" Orthopedic manual surgical instrument (Non-Sterile)

TW: "史賽克" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·STRYKER GMBH·Registered Jul 06, 2015 – Jul 06, 2020Cancelled
Registration details
Analysis ID
a04e30fdecb8c3c470394dc73f320856
License Form
Ministry of Health Medical Device Import No. 015419
Customs Code
DHA09401541902
Company information
Manufacturer
STRYKER GMBH
Manufacturer Country
Switzerland
Product details
Product Type (Level 1)
N Orthopedic devices
Product Type (Level 2)
N4540 Manual osteologic surgery instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 06, 2015
Expiry Date
Jul 06, 2020
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Stryker" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a04e30fdecb8c3c470394dc73f320856 and manufactured by STRYKER GMBH. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including K2M, INC., 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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