Taiwan FDA registration 2aa3b4fcf6e65dcb1bd8129c4aeb5ad1

"美德" manual instrument for general surgery (unsterilized)

TW: "美德" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·HUAIAN MEIDE MEDICAL INSTRUMENTS CO., LTD.·Registered May 28, 2014 – May 28, 2019Cancelled

Registration details

Analysis ID: 2aa3b4fcf6e65dcb1bd8129c4aeb5ad1
Customs Code: DHA09600214601

Company information

Manufacturer: HUAIAN MEIDE MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: China
Authorized Representative: HOSPITAL KEEPER TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Input;; Chinese goods

Dates and status

Registration Date: May 28, 2014
Expiry Date: May 28, 2019
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "美德" manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2aa3b4fcf6e65dcb1bd8129c4aeb5ad1 and manufactured by HUAIAN MEIDE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HOSPITAL KEEPER TECHNOLOGY CO., LTD..

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