Taiwan FDA registration a4acc9d75027bdb2ce8333a7cc5a175e
SINGA Nonpowered flotation therapy mattress (Non-sterile)
TW: 新加 非動力式治療床墊 (未滅菌)
Registration details
- Analysis ID
- a4acc9d75027bdb2ce8333a7cc5a175e
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. a00069
Company information
- Manufacturer
- SINGA TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SINGA TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Non-powered Treatment Mattress (J.5150)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
Dates and status
- Registration Date
- May 19, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for SINGA Nonpowered flotation therapy 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 a4acc9d75027bdb2ce8333a7cc5a175e and manufactured by SINGA TECHNOLOGY CORPORATION. The authorized representative in Taiwan is SINGA TECHNOLOGY CORPORATION.
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