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Pidi Safety Lancet (sterilization) - Taiwan Registration 22840fea4da2fc7930ad7f20681f6e43

Access comprehensive regulatory information for Pidi Safety Lancet (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22840fea4da2fc7930ad7f20681f6e43 and manufactured by HTL-STREFA S.A.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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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22840fea4da2fc7930ad7f20681f6e43
Registration Details
Taiwan FDA Registration: 22840fea4da2fc7930ad7f20681f6e43
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Device Details

Pidi Safety Lancet (sterilization)
TW: ๅฟ…ๅธ ๅฎ‰ๅ…จๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1

Registration Details

22840fea4da2fc7930ad7f20681f6e43

DHA04401143500

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

Input;; QMS/QSD

Dates and Status

Mar 06, 2012

Mar 06, 2027