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Patient tracheal fixture and accessories (unsterilized) - Taiwan Registration 0956d3663265568bdd2d39efa684912f

Access comprehensive regulatory information for Patient tracheal fixture and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0956d3663265568bdd2d39efa684912f and manufactured by DALE MEDICAL PRODUCTS, INC.. The authorized representative in Taiwan is BIOSYSTEMS INC..

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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0956d3663265568bdd2d39efa684912f
Registration Details
Taiwan FDA Registration: 0956d3663265568bdd2d39efa684912f
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Device Details

Patient tracheal fixture and accessories (unsterilized)
TW: "ๆˆด็ˆพ"็—…ๆ‚ฃๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0956d3663265568bdd2d39efa684912f

DHA04400441503

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".

D Anesthesiology

D.5770 ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

May 09, 2006

May 09, 2011

Nov 22, 2012

Cancellation Information

Logged out

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