Taiwan FDA registration 9f154df68176c846470a0d42a964a16e

"Broad Ho" balloon oropharyngeal airway tube (unsterilized)

TW: "廣鎬" 氣囊型口咽氣道管 (未滅菌)

Taiwan·Risk Class 1·OMNIMATE ENTERPRISE CO., LTD.·Registered Dec 21, 2015 – Dec 21, 2020Cancelled

Registration details

Analysis ID: 9f154df68176c846470a0d42a964a16e

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 first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5110 Oropharyngeal airway tubes
Import Information: Domestic

Dates and status

Registration Date: Dec 21, 2015
Expiry Date: Dec 21, 2020
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Broad Ho" balloon oropharyngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f154df68176c846470a0d42a964a16e and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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