Taiwan FDA registration 862b94009e41345d3d4a3ba123d00c84

"Medtronic" Zhu Keli calibration accessory (unsterilized)

TW: "美敦力" 祝可麗校準附件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Covidien llc;; Viant AS&O Holdings, LLC·Registered Mar 15, 2019 – Mar 15, 2029Active
Registration details
Analysis ID
862b94009e41345d3d4a3ba123d00c84
Customs Code
DHA09402019105
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
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
Dates and status
Registration Date
Mar 15, 2019
Expiry Date
Mar 15, 2029
Cancellation Date
Nov 11, 2024
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About this record

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..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITH & NEPHEW INC., ENDOSCOPY DIVISION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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