Taiwan FDA registration daf1b936d4f442674a8ca90866df3d60
"Meida" gram micro-spray nasal sprayer (sterilized)
TW: "美達"克微準-噴鼻器(滅菌)
Taiwan·Risk Class 1·MEDA PHARMA GMBH & CO. KG;; URSAPHARM ARZNEIMITTEL GMBH·Registered Oct 20, 2009 – Oct 20, 2019CancelledRegistration details
- Analysis ID
- daf1b936d4f442674a8ca90866df3d60
- Customs Code
- DHA04400822900
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- AKTIVE ENTERPRISE 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;; Contract manufacturing
Dates and status
- Registration Date
- Oct 20, 2009
- Expiry Date
- Oct 20, 2019
- Cancellation Date
- Aug 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Meida" gram micro-spray nasal sprayer (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number daf1b936d4f442674a8ca90866df3d60 and manufactured by MEDA PHARMA GMBH & CO. KG;; URSAPHARM ARZNEIMITTEL GMBH. The authorized representative in Taiwan is AKTIVE ENTERPRISE CO., LTD..
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