Taiwan FDA registration 89989706fbe3f21b2127eb5075dc966a

Accessories for "Mykewei" endoscopes (unsterilized)

TW: “邁柯唯”內視鏡之附件 (未滅菌)

Taiwan·Risk Class 1·MAQUET CARDIOVASCULAR LLC·Registered Mar 08, 2010 – Mar 08, 2025Expired

Registration details

Analysis ID: 89989706fbe3f21b2127eb5075dc966a
Customs Code: DHA04400860808

Company information

Manufacturer: MAQUET CARDIOVASCULAR LLC
Manufacturer Country: United States
Authorized Representative: GETINGE GROUP TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: import

Dates and status

Registration Date: Mar 08, 2010
Expiry Date: Mar 08, 2025

About this record

Access comprehensive regulatory information for Accessories for "Mykewei" endoscopes (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 89989706fbe3f21b2127eb5075dc966a and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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