Taiwan FDA registration 8350bce7c9219c079ebd56e7728c96da
"Baiduoli" Shengnant electrode is introduced into the system catheter
TW: “百多力”勝能特電極導入系統導管
Taiwan·Risk Class 2·BIOTRONIC SE & CO. KG·Registered May 27, 2020 – May 27, 2030ActiveRegistration details
- Analysis ID
- 8350bce7c9219c079ebd56e7728c96da
- Customs Code
- DHA05603360507
Company information
- Manufacturer
- BIOTRONIC SE & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- BIOTRONIK TAIWAN LIMITED
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
- May 27, 2020
- Expiry Date
- May 27, 2030
About this record
Access comprehensive regulatory information for "Baiduoli" Shengnant electrode is introduced into the system catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8350bce7c9219c079ebd56e7728c96da and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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