Taiwan FDA registration 8b46f1caa31f45d451f0d20711b38a37
"Serenovas" remote guide tube
TW: “賽瑞諾華斯”遠端導引導管
Taiwan·Risk Class 2·Cerenovus, Inc.;; Medos International SARL·Registered Feb 24, 2015 – Feb 24, 2030ActiveRegistration details
- Analysis ID
- 8b46f1caa31f45d451f0d20711b38a37
- Customs Code
- DHA05602702401
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Feb 24, 2015
- Expiry Date
- Feb 24, 2030
About this record
Access comprehensive regulatory information for "Serenovas" remote 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 8b46f1caa31f45d451f0d20711b38a37 and manufactured by Cerenovus, Inc.;; Medos International SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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