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"Apricot Whole" blood collection needle (sterilized) - Taiwan Registration aacb5564f8df8d74e3730fb3c31855f6

Access comprehensive regulatory information for "Apricot Whole" blood collection needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aacb5564f8df8d74e3730fb3c31855f6 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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aacb5564f8df8d74e3730fb3c31855f6
Registration Details
Taiwan FDA Registration: aacb5564f8df8d74e3730fb3c31855f6
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Device Details

"Apricot Whole" blood collection needle (sterilized)
TW: "ๆๅ…จ"ๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1

Registration Details

aacb5564f8df8d74e3730fb3c31855f6

DHA09600375900

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

Apr 22, 2019

Apr 22, 2029