Taiwan FDA registration 6eaa34bcb28501cfdab9e0093e425d9b
"Medtronic" refill set
TW: “美敦力”再充填組套
Taiwan·Risk Class 2·MEDTRONIC NEUROMODULATION;; Medtronic Inc.·Registered Mar 12, 2007 – Mar 12, 2027ActiveRegistration details
- Analysis ID
- 6eaa34bcb28501cfdab9e0093e425d9b
- Customs Code
- DHA00601779705
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5965 Subcutaneous implantable intravascular injection port and guide
- Import Information
- import
Dates and status
- Registration Date
- Mar 12, 2007
- Expiry Date
- Mar 12, 2027
About this record
Access comprehensive regulatory information for "Medtronic" refill set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eaa34bcb28501cfdab9e0093e425d9b and manufactured by MEDTRONIC NEUROMODULATION;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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