Taiwan FDA registration e25837797dc6c8e4ebf5b70f7f5a0480
"Serenovas" guide tube
TW: “賽瑞諾華斯” 導引導管
Taiwan·Risk Class 2·Cerenovus, Inc.;; Medos International SARL·Registered Oct 18, 2013 – Oct 18, 2028ActiveRegistration details
- Analysis ID
- e25837797dc6c8e4ebf5b70f7f5a0480
- Customs Code
- DHA05602543703
Company information
- Manufacturer
- Cerenovus, Inc.;; Medos International SARL
- Manufacturer Country
- Mexico;;Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 18, 2013
- Expiry Date
- Oct 18, 2028
About this record
Access comprehensive regulatory information for "Serenovas" guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e25837797dc6c8e4ebf5b70f7f5a0480 and manufactured by Cerenovus, Inc.;; Medos International SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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