"Interlock" instrument case (Non-Sterile) - Taiwan Registration 10a0561639e315b2f8c0f530003a143b
Access comprehensive regulatory information for "Interlock" instrument case (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 10a0561639e315b2f8c0f530003a143b and manufactured by INTERLOCK MEDIZINTECKNIK GMBH. The authorized representative in Taiwan is KINDMED 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.
Device Details
Registration Details
10a0561639e315b2f8c0f530003a143b
Ministry of Health Medical Device Import No. 019900
DHA09401990008
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
I General and plastic surgical devices
I4800 General Surgery Manual Instrument
Imported from abroad
Dates and Status
Dec 10, 2018
Dec 10, 2023