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"Fuyong" Leisho disposable blood lancet (sterilization) - Taiwan Registration e6fd006493107c706b6d32e6a945f20a

Access comprehensive regulatory information for "Fuyong" Leisho disposable blood 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 e6fd006493107c706b6d32e6a945f20a and manufactured by GMMC. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..

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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e6fd006493107c706b6d32e6a945f20a
Registration Details
Taiwan FDA Registration: e6fd006493107c706b6d32e6a945f20a
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Device Details

"Fuyong" Leisho disposable blood lancet (sterilization)
TW: "็ฆๆฐธ" ้›ท็ขฉๆ‹‹ๆฃ„ๅผๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e6fd006493107c706b6d32e6a945f20a

DHA04401162008

Company Information

Korea, Republic of

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

Input;; QMS/QSD

Dates and Status

Apr 24, 2012

Apr 24, 2017

Dec 13, 2019

Cancellation Information

Logged out

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