Taiwan FDA registration fd0b7cda4ed8923b0c7e7c9464dfb290
"Medtronic" hysteroscopy outflow tubing set (sterilized)
TW: "美敦力" 子宮鏡流出管路組(滅菌)
Taiwan·Risk Class 1·Covidien llc;; Infus Medical Co., Ltd.·Registered Dec 14, 2022 – Dec 14, 2027ActiveRegistration details
- Analysis ID
- fd0b7cda4ed8923b0c7e7c9464dfb290
- Customs Code
- DHA09402298309
Company information
- Manufacturer
- Covidien llc;; Infus Medical Co., Ltd.
- Manufacturer Country
- Thailand;;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
- 輸入;; QMS/QSD;; 委託製造
Dates and status
- Registration Date
- Dec 14, 2022
- Expiry Date
- Dec 14, 2027
- Cancellation Date
- Oct 08, 2024
About this record
Access comprehensive regulatory information for "Medtronic" hysteroscopy outflow tubing set (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd0b7cda4ed8923b0c7e7c9464dfb290 and manufactured by Covidien llc;; Infus Medical Co., Ltd.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices