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"General medical" respirator tubing (unsterilized) - Taiwan Registration 0c007660430fa339bfe57a456ea17074

Access comprehensive regulatory information for "General medical" 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 0c007660430fa339bfe57a456ea17074 and manufactured by PROACT MEDICAL LTD.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS 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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0c007660430fa339bfe57a456ea17074
Registration Details
Taiwan FDA Registration: 0c007660430fa339bfe57a456ea17074
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Device Details

"General medical" respirator tubing (unsterilized)
TW: โ€œๆ™ฎ้†ซโ€ๅ‘ผๅธๅ™จ็ฎก่ทฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0c007660430fa339bfe57a456ea17074

DHA04400939101

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.

D Anesthesiology

D.5975 Respirator Tubing

import

Dates and Status

Oct 21, 2010

Oct 21, 2015

Apr 25, 2018

Cancellation Information

Logged out

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