Taiwan FDA registration 1fb9a876b77aeff0a9c5c7cc83c67f2f

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

TW: "必愛" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BISELLI INSTRUMENTE GMBH & CO. KG.·Registered Mar 17, 2015 – Mar 17, 2020Cancelled
Registration details
Analysis ID
1fb9a876b77aeff0a9c5c7cc83c67f2f
License Form
Ministry of Health Medical Device Import No. 015003
Customs Code
DHA09401500300
Company information
Manufacturer Country
Germany
Authorized Representative
Liren Equipment Factory 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
Mar 17, 2015
Expiry Date
Mar 17, 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 "Biselli" 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 1fb9a876b77aeff0a9c5c7cc83c67f2f and manufactured by BISELLI INSTRUMENTE GMBH & CO. KG.. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BISELLI INSTRUMENTE GMBH & CO. KG., BISELLI INSTRUMENTE GMBH, and 2 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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