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"Gibek" wet ball (artificial nose) - Taiwan Registration baa629fddf84b91b517e00f37d8418a7

Access comprehensive regulatory information for "Gibek" wet ball (artificial nose) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number baa629fddf84b91b517e00f37d8418a7 and manufactured by RUSCH SDN. BHD.. The authorized representative in Taiwan is WESSON MEDICAL 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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baa629fddf84b91b517e00f37d8418a7
Registration Details
Taiwan FDA Registration: baa629fddf84b91b517e00f37d8418a7
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Device Details

"Gibek" wet ball (artificial nose)
TW: "ๅ‰ๅ€ๅ…‹" ๆฝฎๆฟ•็ƒ(ไบบๅทฅ้ผป)
Risk Class 1
Cancelled

Registration Details

baa629fddf84b91b517e00f37d8418a7

DHA04400229700

Company Information

Malaysia

Product Details

A type of pneumatic device that is placed in a tracheostomy (surgical opening of the larynx) or a tracheostomy tube is inserted into the air tube to warm the breath of the patient.

D Anesthesiology

D.5375 Heat and humidity condenser (artificial nose)

import

Dates and Status

Dec 21, 2005

Dec 21, 2010

Oct 29, 2012

Cancellation Information

Logged out

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