"AESCULAP" Nonpowered Neurosurgical Instrument (NON-STERILE)
- Analysis ID
- fdac263c338da3cc5a22d96ecc0ca684
- License Form
- Ministry of Health Medical Device Import No. 016681
- Customs Code
- DHA09401668107
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K4535 Non-powered neurosurgical instruments
- Import Information
- Imported from abroad
- Registration Date
- Jun 21, 2016
- Expiry Date
- Jun 21, 2021
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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.