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"Cottman" ventricular cannula - Taiwan Registration 9524afd1a6431b6cff61f296fd75d8fe

Access comprehensive regulatory information for "Cottman" ventricular cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9524afd1a6431b6cff61f296fd75d8fe and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

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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9524afd1a6431b6cff61f296fd75d8fe
Registration Details
Taiwan FDA Registration: 9524afd1a6431b6cff61f296fd75d8fe
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Device Details

"Cottman" ventricular cannula
TW: "ๆŸฏ็‰นๆ›ผ" ่…ฆๅฎคๅฅ—็ฎก
Risk Class 1
Cancelled

Registration Details

9524afd1a6431b6cff61f296fd75d8fe

DHA04400277204

Company Information

Product Details

A ventricular cannula is used to insert the ventricles for aspiration or injection. This device is often referred to as a ventricular needle.

K Neuroscience

K.4060 Cerebral cannula

import

Dates and Status

Mar 02, 2006

Mar 02, 2011

Nov 27, 2012

Cancellation Information

Logged out

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