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"Stryker" Scrobio classic tibial inner pad - Taiwan Registration 4c0b4c34e749d4dcf0ad4c64fe3ef9d6

Access comprehensive regulatory information for "Stryker" Scrobio classic tibial inner pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c0b4c34e749d4dcf0ad4c64fe3ef9d6 and manufactured by STRYKER IRELAND LIMITED. 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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4c0b4c34e749d4dcf0ad4c64fe3ef9d6
Registration Details
Taiwan FDA Registration: 4c0b4c34e749d4dcf0ad4c64fe3ef9d6
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Device Details

"Stryker" Scrobio classic tibial inner pad
TW: โ€œๅฒ่ณฝๅ…‹โ€ๆ–ฏ้ซ˜ๆฏ”ๆญ็ถ“ๅ…ธ่„›้ชจๅ…งๅขŠ
Risk Class 2
Cancelled

Registration Details

4c0b4c34e749d4dcf0ad4c64fe3ef9d6

DHA00602354006

Company Information

Ireland

Product Details

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

N Orthopedics

N.3565 Knee jointsFemoral metals/polymersPorous coatings of cementless cement

import

Dates and Status

Apr 24, 2012

Apr 24, 2022

May 30, 2022

Cancellation Information

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