Taiwan FDA registration ce495135bdf2d2d2332fe4bf7cfa401d
"Seribis Novus" Seribis Remote Guidance Casing
TW: “賽瑞諾華斯” 賽瑞貝斯遠端導引套管
Taiwan·Risk Class 2·MEDOS INTERNATIONAL SARL;; Cerenovus, Inc.·Registered Nov 15, 2023 – Nov 15, 2028ActiveRegistration details
- Analysis ID
- ce495135bdf2d2d2332fe4bf7cfa401d
- Customs Code
- DHA05603675107
Company information
- Manufacturer
- MEDOS INTERNATIONAL SARL;; Cerenovus, Inc.
- Manufacturer Country
- Mexico;;Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Nov 15, 2023
- Expiry Date
- Nov 15, 2028
About this record
Access comprehensive regulatory information for "Seribis Novus" Seribis Remote Guidance Casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce495135bdf2d2d2332fe4bf7cfa401d and manufactured by MEDOS INTERNATIONAL SARL;; Cerenovus, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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