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Fore Diamond Lancet (unsterilized) - Taiwan Registration d12927612bda0f03a92fd0f75124a105

Access comprehensive regulatory information for Fore Diamond Lancet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d12927612bda0f03a92fd0f75124a105 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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d12927612bda0f03a92fd0f75124a105
Registration Details
Taiwan FDA Registration: d12927612bda0f03a92fd0f75124a105
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Device Details

Fore Diamond Lancet (unsterilized)
TW: ็ฆ็ˆพ้‘ฝ็ŸณๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d12927612bda0f03a92fd0f75124a105

DHA09600382602

Company Information

Product Details

Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Chinese goods;; input

Dates and Status

Jun 05, 2019

Jun 05, 2024