Taiwan FDA registration dbf9d37df0d951b0673e017a79dd611c

"Captain" alternating pressure air mattress (unsterilized)

TW: “尉將”交替式壓力氣墊床 (未滅菌)

Taiwan·Risk Class 1·AIRFLO (XIAMEN) MEDICAL CO. LTD.·Registered Aug 15, 2013 – Aug 15, 2018Cancelled

Registration details

Analysis ID: dbf9d37df0d951b0673e017a79dd611c
Customs Code: DHA09600195605

Company information

Manufacturer: AIRFLO (XIAMEN) MEDICAL CO. LTD.
Manufacturer Country: China
Authorized Representative: MEDICAL-MASTER 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: Aug 15, 2013
Expiry Date: Aug 15, 2018
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Captain" alternating pressure air 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 dbf9d37df0d951b0673e017a79dd611c and manufactured by AIRFLO (XIAMEN) MEDICAL CO. LTD.. The authorized representative in Taiwan is MEDICAL-MASTER CO., LTD..

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