Taiwan FDA registration 8f4f4cd369c398099a76f5f389492a65
"BIOTRONIK" Intracardiac defibrillator magnetic resonance imaging implantable active lead (including accessories)
TW: “百多力” 保心力心內除顫器磁振造影植入式主動導線(包括配件)
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Oct 02, 2024 – Oct 02, 2029ActiveRegistration details
- Analysis ID
- 8f4f4cd369c398099a76f5f389492a65
- Customs Code
- DHA05603742206
Company information
- Manufacturer
- BIOTRONIC SE & CO. KG
- Manufacturer Country
- Germany
- 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.3680 心血管用永久或暫時性之心律調節器電極
- Import Information
- import
Dates and status
- Registration Date
- Oct 02, 2024
- Expiry Date
- Oct 02, 2029
About this record
Access comprehensive regulatory information for "BIOTRONIK" Intracardiac defibrillator magnetic resonance imaging implantable active lead (including accessories) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8f4f4cd369c398099a76f5f389492a65 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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