Taiwan FDA registration 18f77bb9dbb78967381fbe9afa1a6ae4

"Medelux" Manual Instruments for General Surgery (Non-sterilized)

TW: "美德萊克斯" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·Mediflex, a division of Flexbar Machine Corporation·Registered Jan 02, 2024 – Jan 02, 2029Active

Registration details

Analysis ID: 18f77bb9dbb78967381fbe9afa1a6ae4
Customs Code: DHA09402335307

Company information

Manufacturer: Mediflex, a division of Flexbar Machine Corporation
Manufacturer Country: United States
Authorized Representative: MEDITEK LIFESCIENCES CORP.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jan 02, 2024
Expiry Date: Jan 02, 2029

About this record

Access comprehensive regulatory information for "Medelux" Manual Instruments for General Surgery (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18f77bb9dbb78967381fbe9afa1a6ae4 and manufactured by Mediflex, a division of Flexbar Machine Corporation. The authorized representative in Taiwan is MEDITEK LIFESCIENCES CORP..

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