Taiwan FDA registration ad5e2f60f47faa04878ee360ec5e578d

"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·Borun Industrial Co., Ltd. Kaohsiung Factory·Registered Aug 08, 2012 – Aug 08, 2027Active
Registration details
Analysis ID
ad5e2f60f47faa04878ee360ec5e578d
Company information
Manufacturer Country
Taiwan, Province of 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
Domestic
Dates and status
Registration Date
Aug 08, 2012
Expiry Date
Aug 08, 2027
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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 ad5e2f60f47faa04878ee360ec5e578d and manufactured by Borun Industrial Co., Ltd. Kaohsiung Factory. 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 AIRFLO (XIAMEN) MEDICAL CO., LTD, 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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