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Proway Instrument Guide Series (Sterilization) - Taiwan Registration b1fb43e68b7c35714cca2ba45ca68d2c

Access comprehensive regulatory information for Proway Instrument Guide Series (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1fb43e68b7c35714cca2ba45ca68d2c and manufactured by Proway International Limited. The authorized representative in Taiwan is Proway International Limited.

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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b1fb43e68b7c35714cca2ba45ca68d2c
Registration Details
Taiwan FDA Registration: b1fb43e68b7c35714cca2ba45ca68d2c
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Device Details

Proway Instrument Guide Series (Sterilization)
TW: "ๆ™ฎๅจ"ๅ™จๆขฐๅผ•ๅฐŽๅ™จ็ณปๅˆ—(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b1fb43e68b7c35714cca2ba45ca68d2c

DHY04300118506

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment (Manual Instruments for General Surgery [I.4800]).

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Apr 12, 2006

Apr 12, 2021

Sep 23, 2023

Cancellation Information

Logged out

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