“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..
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Device Details
Registration Details
d096d3f91de76e1adf1b8e8d6013039b
Ministry of Health Medical Device Import No. 032060
DHA05603206002
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

