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"Schbil" Xinda blood collection needle - Taiwan Registration 1d64a6c5cd830405c0b695e261536b0e

Access comprehensive regulatory information for "Schbil" Xinda blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d64a6c5cd830405c0b695e261536b0e and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

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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1d64a6c5cd830405c0b695e261536b0e
Registration Details
Taiwan FDA Registration: 1d64a6c5cd830405c0b695e261536b0e
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Device Details

"Schbil" Xinda blood collection needle
TW: โ€œๆ–ฝๅฟ…็ˆพโ€ไฟก้”ๆŽก่ก€้‡
Risk Class 1
Cancelled

Registration Details

1d64a6c5cd830405c0b695e261536b0e

DHA04600036701

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;; Chinese goods

Dates and Status

Apr 27, 2007

Apr 27, 2012

Sep 26, 2016

Cancellation Information

Logged out

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