Taiwan FDA registration 0799e6fd4aa6fe39bb85a2f163bcea30
"Heyang" alternating pressure air mattress (unsterilized)
TW: “禾揚”交替式壓力氣墊床 (未滅菌)
Registration details
- Analysis ID
- 0799e6fd4aa6fe39bb85a2f163bcea30
Company information
- Manufacturer
- SEQUOIA-TWN HEALTHCARE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Heyang Limited
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;; Contract manufacturing
Dates and status
- Registration Date
- Dec 29, 2020
- Expiry Date
- Dec 29, 2025
About this record
Access comprehensive regulatory information for "Heyang" 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 0799e6fd4aa6fe39bb85a2f163bcea30 and manufactured by SEQUOIA-TWN HEALTHCARE CO., LTD.. The authorized representative in Taiwan is Heyang Limited.
This page provides complete technical specifications, regulatory compliance details. 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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