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"AESCULAP" Nonpowered Neurosurgical Instrument (Non-Sterile) - Taiwan Registration ad1c5bfd70181a48c774da708e9e484d

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.

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ad1c5bfd70181a48c774da708e9e484d
Registration Details
Taiwan FDA Registration: ad1c5bfd70181a48c774da708e9e484d
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Device Details

"AESCULAP" Nonpowered Neurosurgical Instrument (Non-Sterile)
TW: "้›…ๆฐ"้žๅ‹•ๅŠ›ๅผ็ฅž็ถ“ๅค–็ง‘็”จๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ad1c5bfd70181a48c774da708e9e484d

Ministry of Health Medical Device Import No. 013327

DHA09401332700

Company Information

Germany

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

Aug 23, 2013

Aug 23, 2028

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