Pure Global

"Febim" non-aerated tourniquet (sterilized) - Taiwan Registration 9017830467eca0b95dba5885c580494a

Access comprehensive regulatory information for "Febim" non-aerated tourniquet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9017830467eca0b95dba5885c580494a and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is NSH MEDICAL 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 Database
Powered by Pure Global AI
89,000+ Devices
9017830467eca0b95dba5885c580494a
Registration Details
Taiwan FDA Registration: 9017830467eca0b95dba5885c580494a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Febim" non-aerated tourniquet (sterilized)
TW: "่ฒปๆฏ”ๅง†"้žๅ……ๆฐฃๅผๆญข่ก€ๅธถ(ๆป…่Œ)
Risk Class 1

Registration Details

9017830467eca0b95dba5885c580494a

DHA09402005204

Company Information

Germany

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

I.5900 ้žๅ……ๆฐฃๅผๆญข่ก€ๅธถ

Input;; QMS/QSD

Dates and Status

Jan 23, 2019

Jan 23, 2029