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Manual instrument for general surgery (unsterilized)  - Taiwan Registration 76d02a87d089e9330da6e4d24e2b356e

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 76d02a87d089e9330da6e4d24e2b356e and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including EUROMI S.A., Gray Surgical, 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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76d02a87d089e9330da6e4d24e2b356e
Registration Details
Taiwan FDA Registration: 76d02a87d089e9330da6e4d24e2b356e
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Device Details

Manual instrument for general surgery (unsterilized) 
TW: “狄成”一般手術用手動式器械 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

76d02a87d089e9330da6e4d24e2b356e

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Domestic

Dates and Status

Mar 18, 2011

Mar 18, 2016

Jul 31, 2018

Cancellation Information

Logged out

未展延而逾期者

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