Taiwan FDA registration 268a3b5dfb6efcb6e6c013636be79b72
"Snowden Pencer" Speculum and Accessories (Non-Sterile)
TW: "史諾頓賓士" 檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION·Registered Sep 06, 2016 – Sep 06, 2021ExpiredRegistration details
- Analysis ID
- 268a3b5dfb6efcb6e6c013636be79b72
- License Form
- Ministry of Health Medical Device Import No. 016963
- Customs Code
- DHA09401696304
Company information
- Manufacturer
- CAREFUSION
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I1800 inspection mirror and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 06, 2016
- Expiry Date
- Sep 06, 2021
About this record
Access comprehensive regulatory information for "Snowden Pencer" Speculum and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 268a3b5dfb6efcb6e6c013636be79b72 and manufactured by CAREFUSION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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