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"Headstar" Airway connector (Non-sterile) - Taiwan Registration a9763891e7b54d39dbcf80303bf9a735

Access comprehensive regulatory information for "Headstar" Airway connector (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a9763891e7b54d39dbcf80303bf9a735 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS 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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a9763891e7b54d39dbcf80303bf9a735
Registration Details
Taiwan FDA Registration: a9763891e7b54d39dbcf80303bf9a735
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Device Details

"Headstar" Airway connector (Non-sterile)
TW: "่ฏๅพท" ๆฐฃ้“้€ฃๆŽฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a9763891e7b54d39dbcf80303bf9a735

Ministry of Health Medical Device Manufacturing No. 007455

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "Airway Connector (D.5810)" of the Measures for the Administration of Medical Devices.

D Devices for anesthesiology

D5810 airway connector

Produced in Taiwan, China

Dates and Status

Oct 01, 2018

Oct 01, 2028