Taiwan FDA registration a8cb302fcb2ecca3bb794e4109ef6be0
"Vidavic" non-respiratory nebulizer (unsterilized)
TW: “維達福”非呼吸用噴霧器(未滅菌)
Taiwan·Risk Class 1·VITALOGRAPH (IRELAND) LIMITED·Registered Aug 21, 2007 – Aug 21, 2012CancelledRegistration details
- Analysis ID
- a8cb302fcb2ecca3bb794e4109ef6be0
- Customs Code
- DHA04400609508
Company information
- Manufacturer
- VITALOGRAPH (IRELAND) LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2007
- Expiry Date
- Aug 21, 2012
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Vidavic" non-respiratory nebulizer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a8cb302fcb2ecca3bb794e4109ef6be0 and manufactured by VITALOGRAPH (IRELAND) LIMITED. The authorized representative in Taiwan is BIOSYSTEMS INC..
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