Taiwan FDA registration 2f4a01ed4dcbd5173cac4cc473aae4a2

"OMNIMATE" NASOPHARYNGEAL AIRWAY (NON-STERILE)

TW: "廣鎬" 鼻咽氣道管 (未滅菌)

Taiwan·Risk Class 1·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered May 30, 2019 – May 30, 2024Expired

Registration details

Analysis ID: 2f4a01ed4dcbd5173cac4cc473aae4a2
License Form: Ministry of Health Medical Device Manufacturing No. 007788

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 Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5100 Nasopharyngeal airway tube
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 30, 2019
Expiry Date: May 30, 2024

About this record

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..

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