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"Keesso" manual orthopedic surgical instruments (unsterilized) - Taiwan Registration dde15bc350281cf5d3da835d62788797

Access comprehensive regulatory information for "Keesso" manual orthopedic surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dde15bc350281cf5d3da835d62788797 and manufactured by GSOURCE, LLC.. The authorized representative in Taiwan is Huixing Co., Ltd.

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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dde15bc350281cf5d3da835d62788797
Registration Details
Taiwan FDA Registration: dde15bc350281cf5d3da835d62788797
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Device Details

"Keesso" manual orthopedic surgical instruments (unsterilized)
TW: โ€œๅŸบ็ดขโ€ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dde15bc350281cf5d3da835d62788797

DHA04401170302

Company Information

United States

Product Details

Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

May 15, 2012

May 15, 2017

Dec 13, 2019

Cancellation Information

Logged out

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