Taiwan FDA registration 5ee0200d804204fbccf22fa27162b05a
"Medtronic" new Kemer infusion system
TW: “美敦力”新可美輸注系統
Registration details
- Analysis ID
- 5ee0200d804204fbccf22fa27162b05a
- Customs Code
- DHA00602386508
Company information
- 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
- Import Information
- import
Dates and status
- Registration Date
- Aug 01, 2012
- Expiry Date
- Aug 01, 2027
About this record
Access comprehensive regulatory information for "Medtronic" new Kemer infusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5ee0200d804204fbccf22fa27162b05a and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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