Pure Global

“AERO” RapidStop Tourniquet (Non-sterile) - Taiwan Registration a5ab2ebbace1791db902f73859887daa

Access comprehensive regulatory information for “AERO” RapidStop Tourniquet (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 a5ab2ebbace1791db902f73859887daa and manufactured by AERO HEALTHCARE US. The authorized representative in Taiwan is CORELEADER BIOTECH 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 Database
Powered by Pure Global AI
89,000+ Devices
a5ab2ebbace1791db902f73859887daa
Registration Details
Taiwan FDA Registration: a5ab2ebbace1791db902f73859887daa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“AERO” RapidStop Tourniquet (Non-sterile)
TW: “艾若” 銳霹速止血帶 (未滅菌)
Risk Class 1
MD

Registration Details

a5ab2ebbace1791db902f73859887daa

Ministry of Health Medical Device Import No. 022732

DHA09402273200

Company Information

United States

Product Details

Limited to the first level identification range of the "non-inflatable tourniquet (I.5900)" of the Measures for the Classification and Grading of Medical Devices.

I General, Plastic Surgery and Dermatology

I5900 Non-inflatable tourniquet

Imported from abroad

Dates and Status

Jan 20, 2022

Jan 20, 2027