Taiwan FDA registration b450835ffbbd6da98f334b3d4a0d16b7

"Mekewei" compensated pipe flow meter (unsterilized)

TW: "邁柯唯"補償式管流量計(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MAQUET GMBH·Registered Oct 05, 2011 – Oct 05, 2021Cancelled
Registration details
Analysis ID
b450835ffbbd6da98f334b3d4a0d16b7
Customs Code
DHA04401090200
Company information
Manufacturer
MAQUET GMBH
Manufacturer Country
Germany
Authorized Representative
GETINGE GROUP TAIWAN 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
Oct 05, 2011
Expiry Date
Oct 05, 2021
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 "Mekewei" compensated pipe 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 b450835ffbbd6da98f334b3d4a0d16b7 and manufactured by MAQUET GMBH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAQUET GMBH, 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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