Taiwan FDA registration 40a03040f053157b69e7e8cad4cc24ff

Manual instrument for general surgery (unsterilized)

TW: "優美痂"一般手術用手動式器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·HUMECA B.V.·Registered Sep 28, 2011 – Sep 28, 2016Cancelled
Registration details
Analysis ID
40a03040f053157b69e7e8cad4cc24ff
Customs Code
DHA04401088401
Company information
Manufacturer
HUMECA B.V.
Manufacturer Country
Netherlands
Authorized Representative
Yangzhi Biotechnology 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, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
import
Dates and status
Registration Date
Sep 28, 2011
Expiry Date
Sep 28, 2016
Cancellation Date
Jul 03, 2018
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 Manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 40a03040f053157b69e7e8cad4cc24ff and manufactured by HUMECA B.V.. The authorized representative in Taiwan is Yangzhi Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including TAKASAGO MEDICAL INDUSTRY CO., LTD., DI CHENG RUBBER INDUSTRIES INC., and 5 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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