Taiwan FDA registration c449df75d2ade28139417371af3e180c
“Sterisets” Alternating Pressure Air Flotation Mattress (Non-Sterile)
TW: “史瑞得” 交替式壓力氣墊床 (未滅菌)
Taiwan·Risk Class 1·MD·STERISETS MEDICAL PRODUCTS·Registered Aug 20, 2020 – Aug 20, 2025ExpiredRegistration details
- Analysis ID
- c449df75d2ade28139417371af3e180c
- License Form
- Ministry of Health Medical Device Import No. 021876
- Customs Code
- DHA09402187603
Company information
- Manufacturer
- STERISETS MEDICAL PRODUCTS
- Manufacturer Country
- Portugal
- Authorized Representative
- CHAMP MEDICS 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)
- J5550 Alternating pressure air mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 20, 2020
- Expiry Date
- Aug 20, 2025
About this record
Access comprehensive regulatory information for “Sterisets” Alternating Pressure Air Flotation Mattress (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c449df75d2ade28139417371af3e180c and manufactured by STERISETS MEDICAL PRODUCTS. The authorized representative in Taiwan is CHAMP MEDICS CO., LTD..
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