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"Cardino" respirator tubing (unsterilized) - Taiwan Registration 49795da10d1f68d0ecc5d4ec5bb08571

Access comprehensive regulatory information for "Cardino" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49795da10d1f68d0ecc5d4ec5bb08571 and manufactured by PRODUCTOS UROLOGOS DE MEXICO, S.A. DE C.V.. The authorized representative in Taiwan is Mitutoyo Medical Equipment 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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49795da10d1f68d0ecc5d4ec5bb08571
Registration Details
Taiwan FDA Registration: 49795da10d1f68d0ecc5d4ec5bb08571
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Device Details

"Cardino" respirator tubing (unsterilized)
TW: "ๅก่ฟช่ซพ" ๅ‘ผๅธๅ™จ็ฎก่ทฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

49795da10d1f68d0ecc5d4ec5bb08571

DHA04400242305

Company Information

Product Details

The respirator line is a device that conducts gas between the ventilation tube and the patient during the patient's ventilation.

D Anesthesiology

D.5975 Respirator Tubing

import

Dates and Status

Dec 29, 2005

Dec 29, 2010

Nov 23, 2012

Cancellation Information

Logged out

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