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“Teleflex” Gibeck Humid-Vent HMEF - Taiwan Registration d096d3f91de76e1adf1b8e8d6013039b

Access comprehensive regulatory information for “Teleflex” Gibeck Humid-Vent HMEF in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d096d3f91de76e1adf1b8e8d6013039b 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.

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d096d3f91de76e1adf1b8e8d6013039b
Registration Details
Taiwan FDA Registration: d096d3f91de76e1adf1b8e8d6013039b
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Device Details

“Teleflex” Gibeck Humid-Vent HMEF
TW: “泰利福”吉倍克細菌病毒過濾潮濕球
Risk Class 2
MD

Registration Details

d096d3f91de76e1adf1b8e8d6013039b

Ministry of Health Medical Device Import No. 032060

DHA05603206002

Company Information

Malaysia

Product Details

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

D Devices for anesthesiology

D5260 Breathing line bacterial filter

Imported from abroad

Dates and Status

Jan 04, 2019

Jan 04, 2024