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"Lianhua" blood lancet (unsterilized) - Taiwan Registration 8cafbaf1ebfdd4a7f2ce2dc92f665a68

Access comprehensive regulatory information for "Lianhua" blood 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 8cafbaf1ebfdd4a7f2ce2dc92f665a68 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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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8cafbaf1ebfdd4a7f2ce2dc92f665a68
Registration Details
Taiwan FDA Registration: 8cafbaf1ebfdd4a7f2ce2dc92f665a68
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Device Details

"Lianhua" blood lancet (unsterilized)
TW: "่ฏ็"ๆŽก่ก€้‡(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8cafbaf1ebfdd4a7f2ce2dc92f665a68

DHA09600347805

Company Information

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

Input;; Chinese goods

Dates and Status

Jul 04, 2018

Jul 04, 2023