Taiwan FDA registration 7e6bd468523353b36edf74734f68b910

"Stryker" Magis detached occlusive roll

TW: “史賽克”瑪琪斯分離式閉塞捲
Taiwan flagTaiwan·Risk Class 3·Stryker Neurovascular·Registered May 03, 2006 – May 03, 2021Cancelled
Registration details
Analysis ID
7e6bd468523353b36edf74734f68b910
Customs Code
DHA00601440002
Company information
Manufacturer Country
Ireland
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Neuroscience
Import Information
import
Dates and status
Registration Date
May 03, 2006
Expiry Date
May 03, 2021
Cancellation Date
Aug 21, 2023
Cancellation information
Status
Logged out
Reason
自請註銷
About this record

Access comprehensive regulatory information for "Stryker" Magis detached occlusive roll in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7e6bd468523353b36edf74734f68b910 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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.

Free DatabasePowered by Pure Global AI89,000+ Devices