Taiwan FDA registration cf4e07409b4ab9cf3ca92452936ee98f
"Gilot's Esmi" Uppas ureters are introduced into the cannula group
TW: “吉洛氏艾斯米”優帕斯輸尿管導入套管組
Taiwan·Risk Class 2·Gyrus ACMI, Inc.·Registered Feb 05, 2015 – Feb 05, 2030ActiveRegistration details
- Analysis ID
- cf4e07409b4ab9cf3ca92452936ee98f
- Customs Code
- DHA05602698309
Company information
- Manufacturer
- Gyrus ACMI, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Feb 05, 2015
- Expiry Date
- Feb 05, 2030
About this record
Access comprehensive regulatory information for "Gilot's Esmi" Uppas ureters are introduced into the cannula group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf4e07409b4ab9cf3ca92452936ee98f and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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