Taiwan FDA registration 5ca64bcbe485c118255c5adad798f56d

"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·K2M, INC.·Registered Jul 15, 2019 – Jul 15, 2024Expired
Registration details
Analysis ID
5ca64bcbe485c118255c5adad798f56d
License Form
Ministry of Health Medical Device Import No. 020652
Customs Code
DHA09402065202
Company information
Manufacturer
K2M, INC.
Manufacturer Country
United States
Product details
Intended Use
Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
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 15, 2019
Expiry Date
Jul 15, 2024
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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 5ca64bcbe485c118255c5adad798f56d and manufactured by K2M, INC.. 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 STRYKER GMBH, 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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