Taiwan FDA registration 150f70b5ed63de1406645a0f9c502ac6

"Maxer" Manual surgical instrument for general use (Non-Sterile)

TW: "麥克斯爾" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MAXER MEDIZINTECHNIK GMBH·Registered Mar 05, 2020 – Mar 05, 2025Expired
Registration details
Analysis ID
150f70b5ed63de1406645a0f9c502ac6
License Form
Ministry of Health Medical Device Import No. 021339
Customs Code
DHA09402133903
Company information
Manufacturer Country
Germany
Authorized Representative
HIGH TOP MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 05, 2020
Expiry Date
Mar 05, 2025
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About this record

Access comprehensive regulatory information for "Maxer" Manual surgical instrument for general use (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 150f70b5ed63de1406645a0f9c502ac6 and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAXER ENDOSCOPY GMBH, 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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