Taiwan FDA registration a9d160707fa0e3ffc3f3fa11dbeb4c06

"Shu double" physiological seawater sprayer (unsterilized)

TW: “舒倍”生理海水噴霧器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SOFIBEL - FUMOUZE LABORATORIES·Registered Nov 02, 2007 – Nov 02, 2017Cancelled
Registration details
Analysis ID
a9d160707fa0e3ffc3f3fa11dbeb4c06
Customs Code
DHA04400627204
Company information
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
Nov 02, 2007
Expiry Date
Nov 02, 2017
Cancellation Date
Nov 28, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Shu double" 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 a9d160707fa0e3ffc3f3fa11dbeb4c06 and manufactured by SOFIBEL - FUMOUZE LABORATORIES. The authorized representative in Taiwan is YUNG HUNG HONG.

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