Taiwan FDA registration dcbeff5bd02b20169842ee5147e8c6e4
"Asiacare" Emergency Push Bed (Unsterilized)
TW: “亞護”急診推床 (未滅菌)
Registration details
- Analysis ID
- dcbeff5bd02b20169842ee5147e8c6e4
Company information
- Manufacturer
- SIGMA-CARE DEVELOPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SIGMA-CARE DEVELOPMENT CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Wheeled Stretcher (J.6910)" first level identification range.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6910 Wheeled Stretcher
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 08, 2009
- Expiry Date
- Jan 08, 2024
About this record
Access comprehensive regulatory information for "Asiacare" Emergency Push Bed (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dcbeff5bd02b20169842ee5147e8c6e4 and manufactured by SIGMA-CARE DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is SIGMA-CARE DEVELOPMENT CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices