Taiwan FDA registration c84841682b43fe536b6b47533d859a4b
"Softmo" Fasima seawater nasal sprayer (unsterilized)
TW: “索芙特摩”法西瑪海水鼻用噴霧器 (未滅菌)
Registration details
- Analysis ID
- c84841682b43fe536b6b47533d859a4b
- Customs Code
- DHA04400789608
Company information
- Manufacturer
- SOFTMER
- Manufacturer Country
- France
- Authorized Representative
- HOCK SHENG TRADING 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
- import
Dates and status
- Registration Date
- Jul 09, 2009
- Expiry Date
- Jul 09, 2014
- 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 "Softmo" Fasima 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 c84841682b43fe536b6b47533d859a4b and manufactured by SOFTMER. The authorized representative in Taiwan is HOCK SHENG TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices