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"Nipro" blood lancet (sterilized) - Taiwan Registration f0916cbc6be7c737745f923e6f756f00

Access comprehensive regulatory information for "Nipro" 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 f0916cbc6be7c737745f923e6f756f00 and manufactured by NIPRO DIAGNOSTICS, INC.;; Tianjin Huahong Technology Co., Ltd.. The authorized representative in Taiwan is Taiwan Nipro Medical Device Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Tianjin Huahong Technology Co., Ltd., and 1 recent registrations in the same category. 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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f0916cbc6be7c737745f923e6f756f00
Registration Details
Taiwan FDA Registration: f0916cbc6be7c737745f923e6f756f00
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Device Details

"Nipro" blood lancet (sterilized)
TW: โ€œๅฐผๆ™ฎๆด›โ€ๆŽก่ก€้‡ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f0916cbc6be7c737745f923e6f756f00

DHA04600192402

Company Information

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

QMS/QSD;; Contract manufacturing;; Input;; Chinese goods

Dates and Status

Jul 02, 2013

Jul 02, 2018

May 19, 2022

Cancellation Information

Logged out

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