Taiwan FDA registration 623ea6ce4f21cc05d688fe6f825c360e

"Guangho" nasal sprayer (unsterilized)

TW: “廣鎬” 鼻腔噴霧器 (未滅菌)

Taiwan·Risk Class 1·OMNIMATE ENTERPRISE CO., LTD.·Registered Apr 15, 2020 – Apr 15, 2030Active

Registration details

Analysis ID: 623ea6ce4f21cc05d688fe6f825c360e

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 of identification scope of the Measures for the Classification and Grading of Medical Devices "ENT Dispensing Devices and Substances Used Together (G.5220)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Apr 15, 2020
Expiry Date: Apr 15, 2030

About this record

Access comprehensive regulatory information for "Guangho" nasal sprayer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 623ea6ce4f21cc05d688fe6f825c360e and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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