Taiwan FDA registration b070233308d0c3171ada83cb4328c1c6
"Serenovas" Emberway suction catheter
TW: “賽瑞諾華斯”恩柏唯抽吸導管
Taiwan·Risk Class 2·Cerenovus, Inc.;; Medos International SARL·Registered Dec 11, 2020 – Dec 11, 2025ExpiredRegistration details
- Analysis ID
- b070233308d0c3171ada83cb4328c1c6
- Customs Code
- DHA05603421601
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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Dec 11, 2020
- Expiry Date
- Dec 11, 2025
About this record
Access comprehensive regulatory information for "Serenovas" Emberway suction catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b070233308d0c3171ada83cb4328c1c6 and manufactured by Cerenovus, Inc.;; Medos International SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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