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"Cottman" Beates shunt - Taiwan Registration ed73195747ba1f6bd9d0563bf07d9e15

Access comprehensive regulatory information for "Cottman" Beates shunt in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed73195747ba1f6bd9d0563bf07d9e15 and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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ed73195747ba1f6bd9d0563bf07d9e15
Registration Details
Taiwan FDA Registration: ed73195747ba1f6bd9d0563bf07d9e15
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Device Details

"Cottman" Beates shunt
TW: โ€œๆŸฏ็‰นๆ›ผโ€่ฒ็‰นๆ–ฏๅˆ†ๆตๅ™จ
Risk Class 2
Cancelled

Registration Details

ed73195747ba1f6bd9d0563bf07d9e15

DHA00602205201

Company Information

United States

Product Details

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

K Neuroscience

K.5550 Central nervous system fluid diverter and its components

import

Dates and Status

Feb 01, 2011

Feb 01, 2016

Aug 01, 2016

Cancellation Information

Logged out

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