Taiwan FDA registration 77202fec1e2acc96c573edae967cb565

"Taiyi" compensated tube flow meter (unsterilized)

TW: "泰儀" 補償式管流量計 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·TECHNOLOGIE MEDICAL S.A.S.·Registered Mar 10, 2017 – Mar 10, 2022Cancelled
Registration details
Analysis ID
77202fec1e2acc96c573edae967cb565
Customs Code
DHA09401758809
Company information
Manufacturer Country
France
Authorized Representative
PHOENIX INSTRUMENT BUSINESS CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the medical equipment management measures "compensated tube flowmeter (D.2340)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.2340 補償式管流量計
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Mar 10, 2017
Expiry Date
Mar 10, 2022
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Taiyi" compensated tube flow meter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77202fec1e2acc96c573edae967cb565 and manufactured by TECHNOLOGIE MEDICAL S.A.S.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TECHNOLOGIE MEDICAL S.A.S., 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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