Taiwan FDA registration e659469e634706ff4188955fc2c2a4ff
Oji nasal aspirator (unsterilized)
TW: 歐治鼻吸鼻器 (未滅菌)
Taiwan·Risk Class 1·STI PLASTICS;; NOVARTIS CONSUMER HEALTH SA·Registered Feb 24, 2014 – Feb 24, 2019CancelledRegistration details
- Analysis ID
- e659469e634706ff4188955fc2c2a4ff
- Customs Code
- DHA09401387008
Company information
- Manufacturer
- STI PLASTICS;; NOVARTIS CONSUMER HEALTH SA
- Manufacturer Country
- France;;Switzerland
- Authorized Representative
- HALEON UK SERVICES LIMITED TAIWAN BRANCH
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Lavage Syringe (J.6960)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6960 Lavage syringe
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2019
- 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 nasal aspirator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e659469e634706ff4188955fc2c2a4ff and manufactured by STI PLASTICS;; NOVARTIS CONSUMER HEALTH SA. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.
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