Taiwan FDA registration 3e5f376f19ccecf4d593256f20a2e103
"Byrdnik" Linas implantable intracardiac defibrillator lead
TW: “拜爾德尼克”霖納思植入式心內除顫器導線
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Jun 30, 2008 – Jun 30, 2013CancelledRegistration details
- Analysis ID
- 3e5f376f19ccecf4d593256f20a2e103
- Customs Code
- DHA00601908700
Company information
- Manufacturer
- BIOTRONIC SE & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- PRO PHARMA TAIWAN INC.
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.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
- Jun 30, 2008
- Expiry Date
- Jun 30, 2013
- Cancellation Date
- Jun 17, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Byrdnik" Linas implantable intracardiac defibrillator lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3e5f376f19ccecf4d593256f20a2e103 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..
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