Taiwan FDA registration d9eb9ea18f9cd904aa9934fd95091a31
“Medtronic” INDIGO HIGH-SPEED OTOLOGIC DRILL
TW: “美敦力”英迪格高速耳科電鑽及配件
Taiwan·Risk Class 2·MD·MEDTRONIC XOMED, INC.·Registered Apr 28, 2017 – Apr 28, 2027ActiveRegistration details
- Analysis ID
- d9eb9ea18f9cd904aa9934fd95091a31
- License Form
- Ministry of Health Medical Device Import No. 029703
- Customs Code
- DHA05602970305
Company information
- Manufacturer
- MEDTRONIC XOMED, 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)
- G ENT device
- Product Type (Level 2)
- G4250 ENT electric or pneumatic surgical drill
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 28, 2017
- Expiry Date
- Apr 28, 2027
About this record
Access comprehensive regulatory information for “Medtronic” INDIGO HIGH-SPEED OTOLOGIC DRILL in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d9eb9ea18f9cd904aa9934fd95091a31 and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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