Taiwan FDA registration 81835a7803ad08b8ef1855ac4a20d93f
"Baiduoli" Avia three-chamber magnetic resonance implantable heart rhythm regulator
TW: “百多力”艾維亞三室型磁振造影植入式心律調節器
Taiwan·Risk Class 2·BIOTRONIC SE & CO. KG·Registered Mar 08, 2013 – Mar 08, 2018CancelledRegistration details
- Analysis ID
- 81835a7803ad08b8ef1855ac4a20d93f
- Customs Code
- DHA00602449404
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.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2013
- Expiry Date
- Mar 08, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baiduoli" Avia three-chamber magnetic resonance implantable heart rhythm regulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81835a7803ad08b8ef1855ac4a20d93f and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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