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"Hengxin" Schulit blood pen (unsterilized) - Taiwan Registration e2019841d4658cd9d4216c3f8e917fe2

Access comprehensive regulatory information for "Hengxin" Schulit blood pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2019841d4658cd9d4216c3f8e917fe2 and manufactured by Hengxin Medical Equipment Co., Ltd. The authorized representative in Taiwan is Hengxin Medical Equipment 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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e2019841d4658cd9d4216c3f8e917fe2
Registration Details
Taiwan FDA Registration: e2019841d4658cd9d4216c3f8e917fe2
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Device Details

"Hengxin" Schulit blood pen (unsterilized)
TW: โ€œ่กกๆฌฃโ€่ˆ’ๅˆฉ็‰นๆŽก่ก€็ญ† (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e2019841d4658cd9d4216c3f8e917fe2

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

Domestic

Dates and Status

May 16, 2014

May 16, 2024

Jun 13, 2022

Cancellation Information

Logged out

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