Taiwan FDA registration e45c2c8b55a0dff686ae38bda5e88395
“BIOTRONIK” Passeo-14 Peripheral Dilatation Catheter
TW: “百多力”帕希爾14周邊氣球擴張導管
Taiwan·Risk Class 2·MD·BIOTRONIK AG·Registered Jun 09, 2015 – Jun 09, 2025ExpiredRegistration details
- Analysis ID
- e45c2c8b55a0dff686ae38bda5e88395
- License Form
- Ministry of Health Medical Device Import No. 027320
- Customs Code
- DHA05602732005
Company information
- Manufacturer
- BIOTRONIK AG
- Manufacturer Country
- Switzerland
- 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 devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2015
- Expiry Date
- Jun 09, 2025
About this record
Access comprehensive regulatory information for “BIOTRONIK” Passeo-14 Peripheral Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e45c2c8b55a0dff686ae38bda5e88395 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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