Taiwan FDA registration cf7d4612f31d975a87ece9e28b1e4b01
“BIOTRONIK” ReCross OTW Dual Lumen GW Support Catheter
TW: “百多力” 力可過雙腔導線支撐導管
Taiwan·Risk Class 2·MD·IMDS Operations B.V.·Registered Oct 10, 2023 – Oct 10, 2028ActiveRegistration details
- Analysis ID
- cf7d4612f31d975a87ece9e28b1e4b01
- License Form
- Ministry of Health Medical Device Import No. 036628
- Customs Code
- DHA05603662808
Company information
- Manufacturer
- IMDS Operations B.V.
- Manufacturer Country
- Netherlands
- 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)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 10, 2023
- Expiry Date
- Oct 10, 2028
About this record
Access comprehensive regulatory information for “BIOTRONIK” ReCross OTW Dual Lumen GW Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf7d4612f31d975a87ece9e28b1e4b01 and manufactured by IMDS Operations B.V.. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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