Taiwan FDA registration f438957191f0dd6fadb6947b2275b2f1
"Pingxiang" nasal sprayer (unsterilized)
TW: “屏翔” 鼻腔噴霧器 (未滅菌)
Taiwan·Risk Class 1·TANNERMEDICO A/S·Registered Oct 17, 2012 – Oct 17, 2017CancelledRegistration details
- Analysis ID
- f438957191f0dd6fadb6947b2275b2f1
- Customs Code
- DHA04401226101
Company information
- Manufacturer
- TANNERMEDICO A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- PICATECH 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
- import
Dates and status
- Registration Date
- Oct 17, 2012
- Expiry Date
- Oct 17, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pingxiang" nasal 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 f438957191f0dd6fadb6947b2275b2f1 and manufactured by TANNERMEDICO A/S. The authorized representative in Taiwan is PICATECH CO., LTD..
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