Pure Global

“OLYMPUS” Single Use Aspiration Needle NA-U403SX - Taiwan Registration 3d8fea8db6e1c0b6ff8a43d7bed1668b

Access comprehensive regulatory information for “OLYMPUS” Single Use Aspiration Needle NA-U403SX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d8fea8db6e1c0b6ff8a43d7bed1668b and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3d8fea8db6e1c0b6ff8a43d7bed1668b
Registration Details
Taiwan FDA Registration: 3d8fea8db6e1c0b6ff8a43d7bed1668b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“OLYMPUS” Single Use Aspiration Needle NA-U403SX
TW: “奧林柏斯”單次使用抽吸生檢針
Risk Class 2
MD

Registration Details

3d8fea8db6e1c0b6ff8a43d7bed1668b

Ministry of Health Medical Device Import No. 034289

DHA05603428902

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT device

G4680 Bronchoscope (soft or rigid) and accessories

Imported from abroad

Dates and Status

Feb 18, 2021

Feb 18, 2026