Taiwan FDA registration dfdf060f87232741ae4472ae7df4f60a
"Glaxo" pandelin aspiration aid (unsterilized)
TW: “葛蘭素”泛得林吸藥輔助器(未滅菌)
Taiwan·Risk Class 1·SMITHKLINE BEECHAM LIMITED·Registered Nov 15, 2012 – Nov 15, 2017CancelledRegistration details
- Analysis ID
- dfdf060f87232741ae4472ae7df4f60a
- Customs Code
- DHA04401237309
Company information
- Manufacturer
- SMITHKLINE BEECHAM LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLAXOSMITHKLINE FAR EAST B.V., TAIWAN BRANCH (NETHERLANDS)
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
- Nov 15, 2012
- Expiry Date
- Nov 15, 2017
- Cancellation Date
- Mar 06, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Glaxo" pandelin aspiration aid (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfdf060f87232741ae4472ae7df4f60a and manufactured by SMITHKLINE BEECHAM LIMITED. The authorized representative in Taiwan is GLAXOSMITHKLINE FAR EAST B.V., TAIWAN BRANCH (NETHERLANDS).
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