Taiwan FDA registration fccafaf4b0b127205d3360165ccb3f62
"Medtronic" PIDIA parathyroid detection system
TW: “美敦力”匹迪艾副甲狀腺偵測系統
Taiwan·Risk Class 2·Medtronic Xomed, Inc.·Registered Nov 11, 2024 – Nov 11, 2029ActiveRegistration details
- Analysis ID
- fccafaf4b0b127205d3360165ccb3f62
- Customs Code
- DHA05603734603
Company information
- Manufacturer
- Medtronic Xomed, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- This system is used as an adjunct to assist in the identification of parathyroid tissue that has been visually localized by the physician and is used in adult patients aged 18 years or older.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.9999 Miscellaneous
- Import Information
- import
Dates and status
- Registration Date
- Nov 11, 2024
- Expiry Date
- Nov 11, 2029
About this record
Access comprehensive regulatory information for "Medtronic" PIDIA parathyroid detection system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fccafaf4b0b127205d3360165ccb3f62 and manufactured by Medtronic Xomed, Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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