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Wuxi Xinda blood collection device - Taiwan Registration 3dcd7cecc73e5fb9f6109d9d13f3b33c

Access comprehensive regulatory information for Wuxi Xinda blood collection device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3dcd7cecc73e5fb9f6109d9d13f3b33c and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is APEX BIOTECHNOLOGY 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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3dcd7cecc73e5fb9f6109d9d13f3b33c
Registration Details
Taiwan FDA Registration: 3dcd7cecc73e5fb9f6109d9d13f3b33c
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Device Details

Wuxi Xinda blood collection device
TW: ็„ก้Œซไฟก้”ๆŽก่ก€ๅ™จ
Risk Class 1
Cancelled

Registration Details

3dcd7cecc73e5fb9f6109d9d13f3b33c

DHA04600015502

Company Information

Product Details

Limited to the first level identification range 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

Mar 31, 2006

Mar 31, 2011

Jan 21, 2013

Cancellation Information

Logged out

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