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AICA Lancet (sterilized) - Taiwan Registration 44cc659d7a9d5f5e327a87cd5c6db73f

Access comprehensive regulatory information for AICA 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 44cc659d7a9d5f5e327a87cd5c6db73f 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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44cc659d7a9d5f5e327a87cd5c6db73f
Registration Details
Taiwan FDA Registration: 44cc659d7a9d5f5e327a87cd5c6db73f
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Device Details

AICA Lancet (sterilized)
TW: ๆ„›ๅ…‹ ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1

Registration Details

44cc659d7a9d5f5e327a87cd5c6db73f

DHA09600364600

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;; QMS/QSD;; input

Dates and Status

Dec 21, 2018

Dec 21, 2028