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"Stryker" Magis detached occlusive roll - Taiwan Registration 7e6bd468523353b36edf74734f68b910

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.

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7e6bd468523353b36edf74734f68b910
Registration Details
Taiwan FDA Registration: 7e6bd468523353b36edf74734f68b910
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Device Details

"Stryker" Magis detached occlusive roll
TW: โ€œๅฒ่ณฝๅ…‹โ€็‘ช็ชๆ–ฏๅˆ†้›ขๅผ้–‰ๅกžๆฒ
Risk Class 3
Cancelled

Registration Details

7e6bd468523353b36edf74734f68b910

DHA00601440002

Company Information

Ireland

Product Details

For details, it is Chinese approved copy of the imitation order

K Neuroscience

import

Dates and Status

May 03, 2006

May 03, 2021

Aug 21, 2023

Cancellation Information

Logged out

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