Taiwan FDA registration 2fe7b91ae6f2af27865a58d0e274fd7b
"Twiz" portable stretcher (unsterilized)
TW: "特維士" 手提式擔架 (未滅菌)
Registration details
- Analysis ID
- 2fe7b91ae6f2af27865a58d0e274fd7b
- Customs Code
- DHA08402051700
Company information
- Manufacturer
- TRAVERSE RESCUE
- Manufacturer Country
- Canada
- Authorized Representative
- ADEPT GENERAL CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the "portable stretcher (J.6900)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6900 Hand-held stretcher
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Twiz" portable stretcher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fe7b91ae6f2af27865a58d0e274fd7b and manufactured by TRAVERSE RESCUE. The authorized representative in Taiwan is ADEPT GENERAL CORP..
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