Taiwan FDA registration a5684e9f4e7c97ca34cfbce0eeed6a66

"Beren" alternating pressure mattress (unsterilized)

TW: “柏倫”交替式壓力氣墊床 (未滅菌)

Taiwan·Risk Class 1·AIRFLO (XIAMEN) MEDICAL CO. LTD.·Registered Dec 20, 2012 – Dec 20, 2022Cancelled

Registration details

Analysis ID: a5684e9f4e7c97ca34cfbce0eeed6a66
Customs Code: DHA04600181102

Company information

Manufacturer: AIRFLO (XIAMEN) MEDICAL CO. LTD.
Manufacturer Country: China
Authorized Representative: GRAND HEALTHCARE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5550 交替式壓力氣墊床
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Dec 20, 2012
Expiry Date: Dec 20, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Beren" alternating pressure mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5684e9f4e7c97ca34cfbce0eeed6a66 and manufactured by AIRFLO (XIAMEN) MEDICAL CO. LTD.. The authorized representative in Taiwan is GRAND HEALTHCARE CO., LTD..

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