Taiwan FDA registration 098e2ee567df75d347b2cadbb0741367

"McKewei" artificial blood vessels

TW: “邁柯唯”人工血管
Taiwan flagTaiwan·Risk Class 2·MAQUET CARDIOVASCULAR LLC;; VISAMED GmbH·Registered May 02, 2012 – May 02, 2022Cancelled
Registration details
Analysis ID
098e2ee567df75d347b2cadbb0741367
Customs Code
DHA00602348906
Company information
Manufacturer Country
United States;;Germany
Authorized Representative
GETINGE GROUP TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.3450 血管移植彌補物
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
May 02, 2012
Expiry Date
May 02, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "McKewei" artificial blood vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 098e2ee567df75d347b2cadbb0741367 and manufactured by MAQUET CARDIOVASCULAR LLC;; VISAMED 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 CARDIOVASCULAR LLC;; VISAMED 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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