"AESCULAP" Nonpowered Neurosurgical Instrument (Non-Sterile)
Taiwan·Risk Class 1·MD·AESCULAP AG·Registered Aug 23, 2013 – Aug 23, 2028Active- Analysis ID
- ad1c5bfd70181a48c774da708e9e484d
- License Form
- Ministry of Health Medical Device Import No. 013327
- Customs Code
- DHA09401332700
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN 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
- Aug 23, 2013
- Expiry Date
- Aug 23, 2028
Top companies providing products similar to ""AESCULAP" Nonpowered Neurosurgical Instrument (Non-Sterile)"
Recently registered similar products
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 ad1c5bfd70181a48c774da708e9e484d and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN 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.