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"Gaydon" Ezik-style carbon dioxide fog blower - Taiwan Registration af5208d514b8d44381d67bd35f929a68

Access comprehensive regulatory information for "Gaydon" Ezik-style carbon dioxide fog blower in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af5208d514b8d44381d67bd35f929a68 and manufactured by GUIDANT CORPORATION CARDIAC SURGERY. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.

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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af5208d514b8d44381d67bd35f929a68
Registration Details
Taiwan FDA Registration: af5208d514b8d44381d67bd35f929a68
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Device Details

"Gaydon" Ezik-style carbon dioxide fog blower
TW: "่“‹็™ป" ่‰พ้ฝŠๅ…‹ๅผไบŒๆฐงๅŒ–็ขณๅน้œงๅ™จ
Risk Class 1
Cancelled

Registration Details

af5208d514b8d44381d67bd35f929a68

DHA04400024905

Company Information

United States

Product Details

It is used in coronary artery anastomosis surgery to remove blood from the anastomosis to increase the visibility of the surgical field.

J General hospital and personal use equipment

import

Dates and Status

Jul 21, 2005

Jul 21, 2010

Nov 16, 2012

Cancellation Information

Logged out

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