"OMNIMATE" NASOPHARYNGEAL AIRWAY (NON-STERILE) - Taiwan Registration 2f4a01ed4dcbd5173cac4cc473aae4a2
Access comprehensive regulatory information for "OMNIMATE" NASOPHARYNGEAL AIRWAY (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 2f4a01ed4dcbd5173cac4cc473aae4a2 and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE 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.
Device Details
Registration Details
2f4a01ed4dcbd5173cac4cc473aae4a2
Ministry of Health Medical Device Manufacturing No. 007788
Product Details
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
D Devices for anesthesiology
D5100 Nasopharyngeal airway tube
Produced in Taiwan, China
Dates and Status
May 30, 2019
May 30, 2024

