Taiwan FDA registration 2ce9f685c69e4ffc18caa7ad717dbd19

"Dufner" Manual Surgical Instrument for General Use (Non-Sterile)

TW: "杜芙娜" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DUFNER INSTRUMENTE GMBH Medizintechnik·Registered Mar 01, 2017 – Mar 01, 2027Active
Registration details
Analysis ID
2ce9f685c69e4ffc18caa7ad717dbd19
License Form
Ministry of Health Medical Device Import No. 017538
Customs Code
DHA09401753807
Company information
Manufacturer Country
Germany
Authorized Representative
Huixing 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 01, 2017
Expiry Date
Mar 01, 2027
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About this record

Access comprehensive regulatory information for "Dufner" 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 2ce9f685c69e4ffc18caa7ad717dbd19 and manufactured by DUFNER INSTRUMENTE GMBH Medizintechnik. The authorized representative in Taiwan is Huixing Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DUFNER INSTRUMENTE GMBH, DUFNER INSTRUMENT GMBH, and 3 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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