Taiwan FDA registration 753720ee979ba104924255ab5ca2ee97

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

TW: "達夫納" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DUFNER INSTRUMENTE GMBH·Registered Nov 13, 2015 – Nov 13, 2020Cancelled
Registration details
Analysis ID
753720ee979ba104924255ab5ca2ee97
License Form
Ministry of Health Medical Device Import No. 015858
Customs Code
DHA09401585802
Company information
Manufacturer Country
Germany
Authorized Representative
Changjing Instrument Co., Ltd
Product details
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
Nov 13, 2015
Expiry Date
Nov 13, 2020
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 753720ee979ba104924255ab5ca2ee97 and manufactured by DUFNER INSTRUMENTE GMBH. The authorized representative in Taiwan is Changjing Instrument Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 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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