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Diaphragmatic needle in the "Baylis" room - Taiwan Registration ac9e1ef242b7fbc2d63145e5239452da

Access comprehensive regulatory information for Diaphragmatic needle in the "Baylis" room in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac9e1ef242b7fbc2d63145e5239452da and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is CHINA SPRING TRADING 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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ac9e1ef242b7fbc2d63145e5239452da
Registration Details
Taiwan FDA Registration: ac9e1ef242b7fbc2d63145e5239452da
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Device Details

Diaphragmatic needle in the "Baylis" room
TW: โ€œ่ฒๅˆฉๆ–ฏโ€ๆˆฟไธญ่†ˆ็ฉฟๅˆบ้‡
Risk Class 2
Cancelled

Registration Details

ac9e1ef242b7fbc2d63145e5239452da

DHA00601984003

Company Information

Canada

Product Details

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

E Cardiovascular Medicine Science

E.5175 Panectomy Conduit

import

Dates and Status

May 12, 2009

May 12, 2014

Jan 09, 2017

Cancellation Information

Logged out

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