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Schbir blood lancet - Taiwan Registration a97b914c5640b6e7a30580f0cde40435

Access comprehensive regulatory information for Schbir blood lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a97b914c5640b6e7a30580f0cde40435 and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is BIONIME 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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a97b914c5640b6e7a30580f0cde40435
Registration Details
Taiwan FDA Registration: a97b914c5640b6e7a30580f0cde40435
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Device Details

Schbir blood lancet
TW: ๆ–ฝๆฏ”็ˆพๆŽก่ก€้‡
Risk Class 1
Cancelled

Registration Details

a97b914c5640b6e7a30580f0cde40435

DHA04600009303

Company Information

Product Details

The skin is punctured and a small blood sample is collected.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Jan 10, 2006

Jan 10, 2011

Oct 29, 2012

Cancellation Information

Logged out

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