Taiwan FDA registration 4a58110a93e6aea5c9206535bc045291

"Beren" alternating pressure air mattress

TW: "柏倫" 交替式壓力氣墊床
Taiwan flagTaiwan·Risk Class 1·XIAMEN HEALTH ELECTRIC CO., LTD.·Registered Mar 31, 2006 – Mar 31, 2016Cancelled
Registration details
Analysis ID
4a58110a93e6aea5c9206535bc045291
Customs Code
DHA04600015703
Company information
Manufacturer Country
China
Authorized Representative
GRAND HEALTHCARE CO., LTD.
Product details
Intended Use
限醫療器材管理辦法「交替式壓力氣墊床(Alternating pressure air flotation mattress)[J.5550]第一等級鑑別範圍.
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
import
Dates and status
Registration Date
Mar 31, 2006
Expiry Date
Mar 31, 2016
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Beren" alternating pressure air mattress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a58110a93e6aea5c9206535bc045291 and manufactured by XIAMEN HEALTH ELECTRIC CO., LTD.. The authorized representative in Taiwan is GRAND HEALTHCARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Borun Industrial Co., Ltd. Kaohsiung Factory, AIRFLO (XIAMEN) MEDICAL CO., LTD, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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