"AESCULAP" Nonpowered Neurosurgical Instrument (NON-STERILE) - Taiwan Registration fdac263c338da3cc5a22d96ecc0ca684
Access comprehensive regulatory information for "AESCULAP" Nonpowered Neurosurgical Instrument (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 fdac263c338da3cc5a22d96ecc0ca684 and manufactured by AESCULAP AG. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AESCULAP AG, and 1 recent registrations in the same category. 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
fdac263c338da3cc5a22d96ecc0ca684
Ministry of Health Medical Device Import No. 016681
DHA09401668107
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
K Devices for neuroscience
K4535 Non-powered neurosurgical instruments
Imported from abroad
Dates and Status
Jun 21, 2016
Jun 21, 2021