Taiwan FDA registration b857c7f131d72f2e88b58ad0a4c8bcbb

"Broad Ho" balloon type oropharyngeal airway tube (sterilized)

TW: "廣鎬" 氣囊型口咽氣道管 (滅菌)

Taiwan·Risk Class 1·OMNIMATE ENTERPRISE CO., LTD.·Registered Aug 26, 2016 – Aug 26, 2026Active

Registration details

Analysis ID: b857c7f131d72f2e88b58ad0a4c8bcbb

Company information

Manufacturer: OMNIMATE ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: OMNIMATE ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the classification and grading management method of medical equipment, oropharyngeal airway canal (D.5110) first grade identification range.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5110 Oropharyngeal airway tubes
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Aug 26, 2016
Expiry Date: Aug 26, 2026

About this record

Access comprehensive regulatory information for "Broad Ho" balloon type oropharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b857c7f131d72f2e88b58ad0a4c8bcbb 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.