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"Shin Sheng" Lancing device (Non-Sterile) - Taiwan Registration 64492a2cce6ca5e0241823d12678c6e5

Access comprehensive regulatory information for "Shin Sheng" Lancing device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64492a2cce6ca5e0241823d12678c6e5 and manufactured by GMMC. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL 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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64492a2cce6ca5e0241823d12678c6e5
Registration Details
Taiwan FDA Registration: 64492a2cce6ca5e0241823d12678c6e5
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Device Details

"Shin Sheng" Lancing device (Non-Sterile)
TW: "ๅนธ็”Ÿ" ๆŽก่ก€็ญ† (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

64492a2cce6ca5e0241823d12678c6e5

Ministry of Health Medical Device Import No. 013811

DHA09401381105

Company Information

Korea, Republic of

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jan 27, 2014

Jan 27, 2019

Jun 07, 2022

Cancellation Information

Logged out

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