Taiwan FDA registration e90cd590fb605ee437926d19264190d8

"Beren" alternating pressure air mattress (unsterilized)

TW: “柏倫”交替式壓力氣墊床(未滅菌)
Taiwan flagTaiwan·Risk Class 1·AIRFLO (XIAMEN) MEDICAL CO., LTD·Registered May 09, 2023 – May 09, 2028Active
Registration details
Analysis ID
e90cd590fb605ee437926d19264190d8
Customs Code
DHA09600476602
Company information
Manufacturer Country
China
Authorized Representative
GRAND HEALTHCARE CO., LTD.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.
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
QMS/QSD;; Chinese goods;; input
Dates and status
Registration Date
May 09, 2023
Expiry Date
May 09, 2028
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About this record

Access comprehensive regulatory information for "Beren" 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 e90cd590fb605ee437926d19264190d8 and manufactured by AIRFLO (XIAMEN) MEDICAL CO., LTD. The authorized representative in Taiwan is GRAND HEALTHCARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Borun Industrial Co., Ltd. Kaohsiung Factory, and 1 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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