Taiwan FDA registration 0b0daebb7e200f121c3f90368be1ff8b

"Delsa" suction suction nasal sprayer (sterilization)

TW: “德爾薩”吸適森鼻用噴霧器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·URSAPHARM ARZNEIMITTEL GMBH·Registered Dec 04, 2008 – Dec 04, 2018Cancelled
Registration details
Analysis ID
0b0daebb7e200f121c3f90368be1ff8b
Customs Code
DHA04400729406
Company information
Manufacturer Country
Germany
Authorized Representative
CHI FU 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
Input;; QMS/QSD
Dates and status
Registration Date
Dec 04, 2008
Expiry Date
Dec 04, 2018
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Delsa" suction suction nasal sprayer (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b0daebb7e200f121c3f90368be1ff8b and manufactured by URSAPHARM ARZNEIMITTEL GMBH. The authorized representative in Taiwan is CHI FU 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