Taiwan FDA registration 06f416820943c0e567b82b85e1364843

"OMNIMATE" LARYNGEAL MASK AIRWAY (NON-STERILE)

TW: "廣鎬" 喉罩 (未滅菌)

Taiwan·Risk Class 1·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered Sep 20, 2018 – Sep 20, 2023Expired

Registration details

Analysis ID: 06f416820943c0e567b82b85e1364843
License Form: Ministry of Health Medical Device Manufacturing No. 007444

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 Devices for anesthesiology
Product Type (Level 2): D5110 Oropharyngeal airway tube
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Sep 20, 2018
Expiry Date: Sep 20, 2023

About this record

Access comprehensive regulatory information for "OMNIMATE" LARYNGEAL MASK 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 06f416820943c0e567b82b85e1364843 and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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