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"Lianxiang" blood lancet (sterilized) - Taiwan Registration 6d1a3deefb58d8352a95e8b54de20ab4

Access comprehensive regulatory information for "Lianxiang" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6d1a3deefb58d8352a95e8b54de20ab4 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is LEISON BIOTECH CO., LTD..

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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6d1a3deefb58d8352a95e8b54de20ab4
Registration Details
Taiwan FDA Registration: 6d1a3deefb58d8352a95e8b54de20ab4
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Device Details

"Lianxiang" blood lancet (sterilized)
TW: "้€ฃ้™ž" ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1

Registration Details

6d1a3deefb58d8352a95e8b54de20ab4

DHA09600327109

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

QMS/QSD;; Chinese goods;; input

Dates and Status

Nov 16, 2017

Nov 16, 2027