Pure Global

ApexBio Lancing Device (Non-sterile) - Taiwan Registration fef70dad3ad08ccb4abf9c024a339583

Access comprehensive regulatory information for ApexBio Lancing Device (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fef70dad3ad08ccb4abf9c024a339583 and manufactured by OWEN MUMFORD LIMITED. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
fef70dad3ad08ccb4abf9c024a339583
Registration Details
Taiwan FDA Registration: fef70dad3ad08ccb4abf9c024a339583
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

ApexBio Lancing Device (Non-sterile)
TW: ไบ”้ผŽๆŽก่ก€ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fef70dad3ad08ccb4abf9c024a339583

Ministry of Health Medical Device Import No. 018902

DHA09401890207

Company Information

United Kingdom

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 and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Mar 16, 2018

Mar 16, 2023