Taiwan FDA registration 78b619e46c0f6f2bd066d2af3e037e76

"Leitch" non-inflatable tourniquet (unsterilized)

TW: "萊奇"非充氣式止血帶(未滅菌)
Taiwan flagTaiwan·Risk Class 1·EMSTREAM CORPORATION·Registered Feb 04, 2013 – Feb 04, 2018Cancelled
Registration details
Analysis ID
78b619e46c0f6f2bd066d2af3e037e76
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
ADEPT GENERAL CORP.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.5900 非充氣式止血帶
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Feb 04, 2013
Expiry Date
Feb 04, 2018
Cancellation Date
Nov 20, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Leitch" non-inflatable tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 78b619e46c0f6f2bd066d2af3e037e76 and manufactured by EMSTREAM CORPORATION. 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