Taiwan FDA registration 2c1837e0988f48db1b3e51ee6176e25b
"Baidoli" Enoff controlled sheath tube
TW: "百多力"艾諾芙可控式鞘管
Registration details
- Analysis ID
- 2c1837e0988f48db1b3e51ee6176e25b
- Customs Code
- DHA05603533004
Company information
- Manufacturer
- ACUTUS MEDICAL, INC
- Manufacturer Country
- United States
- Authorized Representative
- BIOTRONIK TAIWAN LIMITED
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.1280 controllable guide
- Import Information
- import
Dates and status
- Registration Date
- Mar 17, 2022
- Expiry Date
- Mar 17, 2027
About this record
Access comprehensive regulatory information for "Baidoli" Enoff controlled sheath tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2c1837e0988f48db1b3e51ee6176e25b and manufactured by ACUTUS MEDICAL, INC. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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