Taiwan FDA registration cbcf27483e15ad5bc1d9f3f8359bd9cc
Oji nose sea nose sprayer (unsterilized)
TW: 歐治鼻海水鼻用噴霧器（未滅菌）
Taiwan·Risk Class 1·NOVARTIS CONSUMER HEALTH SA;; SPPH·Registered Aug 09, 2010 – Aug 09, 2020CancelledRegistration details
- Analysis ID
- cbcf27483e15ad5bc1d9f3f8359bd9cc
- Customs Code
- DHA04400905702
Company information
- Manufacturer
- NOVARTIS CONSUMER HEALTH SA;; SPPH
- Manufacturer Country
- France;;Switzerland
- Authorized Representative
- HALEON UK SERVICES LIMITED TAIWAN BRANCH
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
- import
Dates and status
- Registration Date
- Aug 09, 2010
- Expiry Date
- Aug 09, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Oji nose sea nose 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 cbcf27483e15ad5bc1d9f3f8359bd9cc and manufactured by NOVARTIS CONSUMER HEALTH SA;; SPPH. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.
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