Taiwan FDA registration 703a4455a1f3438683c195882af9773c
"Sube" physiological seawater sprayer (unsterilized)
TW: "舒倍"生理海水噴霧器(未滅菌)
Taiwan·Risk Class 1·SOFIBEL - FUMOUZE LABORATORIES·Registered May 24, 2011 – May 24, 2016CancelledRegistration details
- Analysis ID
- 703a4455a1f3438683c195882af9773c
- Customs Code
- DHA04401038802
Company information
- Manufacturer
- SOFIBEL - FUMOUZE LABORATORIES
- Manufacturer Country
- France
- Authorized Representative
- YUNG HUNG HONG
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
- May 24, 2011
- Expiry Date
- May 24, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Sube" physiological seawater 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 703a4455a1f3438683c195882af9773c and manufactured by SOFIBEL - FUMOUZE LABORATORIES. The authorized representative in Taiwan is YUNG HUNG HONG.
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