Taiwan FDA registration 2d25aea22be9d863d4bdf4821fb7fa18

"Novartis" Ouji Nose Physiological Seawater Nasal Sprayer (Unsterilized)

TW: “諾華”歐治鼻生理海水鼻用噴霧器 (未滅菌)

Taiwan·Risk Class 1·NOVARTIS CONSUMER HEALTH SA;; SPPH·Registered Jul 05, 2011 – Jul 05, 2016Cancelled

Registration details

Analysis ID: 2d25aea22be9d863d4bdf4821fb7fa18
Customs Code: DHA04401053907

Company information

Manufacturer: NOVARTIS CONSUMER HEALTH SA;; SPPH
Manufacturer Country: France;;Switzerland
Authorized Representative: NOVARTIS (TAIWAN) CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (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: Input;; Contract manufacturing

Dates and status

Registration Date: Jul 05, 2011
Expiry Date: Jul 05, 2016
Cancellation Date: Aug 14, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Novartis" Ouji Nose Physiological Seawater 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 2d25aea22be9d863d4bdf4821fb7fa18 and manufactured by NOVARTIS CONSUMER HEALTH SA;; SPPH. The authorized representative in Taiwan is NOVARTIS (TAIWAN) CO., LTD..

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