Pure Global

BD Snowden Pencer Retractor (Non-Sterile) - Taiwan Registration e78488f61be05d5daa4ef5d9daf4512f

Access comprehensive regulatory information for BD Snowden Pencer Retractor (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 e78488f61be05d5daa4ef5d9daf4512f and manufactured by CAREFUSION. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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
e78488f61be05d5daa4ef5d9daf4512f
Registration Details
Taiwan FDA Registration: e78488f61be05d5daa4ef5d9daf4512f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

BD Snowden Pencer Retractor (Non-Sterile)
TW: BD ็‰ฝๅผ•ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e78488f61be05d5daa4ef5d9daf4512f

Ministry of Health Medical Device Import No. 020847

DHA09402084704

Company Information

United States

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

Sep 11, 2019

Sep 11, 2024