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"AIKE" blood lancet (sterilized) - Taiwan Registration 10c17dbcf2d843de781e81b8890c7683

Access comprehensive regulatory information for "AIKE" 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 10c17dbcf2d843de781e81b8890c7683 and manufactured by Qiaolian Technology Co., Ltd. Nankan No. 2 Factory. 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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10c17dbcf2d843de781e81b8890c7683
Registration Details
Taiwan FDA Registration: 10c17dbcf2d843de781e81b8890c7683
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Device Details

"AIKE" blood lancet (sterilized)
TW: "ๆ„›ๅ…‹" ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

10c17dbcf2d843de781e81b8890c7683

Company Information

Taiwan, Province of China

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

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Dates and Status

Mar 21, 2017

Mar 21, 2022

Apr 12, 2024

Cancellation Information

Logged out

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