"Medtronic" Zhu Keli calibration accessory (unsterilized)
- Analysis ID
- 862b94009e41345d3d4a3ba123d00c84
- Customs Code
- DHA09402019105
- Manufacturer
- Covidien llc;; Viant AS&O Holdings, LLC
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- Limited to the classification and grading management method of medical equipment "hysteroscopic perfusion device (L.1700)" the first level identification range.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1700 子宮鏡灌入器
- Import Information
- Contract manufacturing;; input
- Registration Date
- Mar 15, 2019
- Expiry Date
- Mar 15, 2029
- Cancellation Date
- Nov 11, 2024
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Access comprehensive regulatory information for "Medtronic" Zhu Keli calibration accessory (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 862b94009e41345d3d4a3ba123d00c84 and manufactured by Covidien llc;; Viant AS&O Holdings, LLC. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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