Pure Global

“RUSCH” SILASIL foley catheters - Taiwan Registration 4f31683ede5d0dcce99ee4f0e2fe419e

Access comprehensive regulatory information for “RUSCH” SILASIL foley catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f31683ede5d0dcce99ee4f0e2fe419e and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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
4f31683ede5d0dcce99ee4f0e2fe419e
Registration Details
Taiwan FDA Registration: 4f31683ede5d0dcce99ee4f0e2fe419e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“RUSCH” SILASIL foley catheters
TW: “路希”希拉夕爾導尿管
Risk Class 2
MD
Cancelled

Registration Details

4f31683ede5d0dcce99ee4f0e2fe419e

Ministry of Health Medical Device Import No. 027387

DHA05602738701

Company Information

Malaysia

Product Details

H Gastroenterology-urology devices

H5130 Urinary catheters and their accessories

Imported from abroad

Dates and Status

May 13, 2015

May 13, 2020

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期