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“Rusch” Laryngoflex Tube - Taiwan Registration d3f125cdf3fb919908aabfe193b52d3b

Access comprehensive regulatory information for “Rusch” Laryngoflex Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3f125cdf3fb919908aabfe193b52d3b and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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d3f125cdf3fb919908aabfe193b52d3b
Registration Details
Taiwan FDA Registration: d3f125cdf3fb919908aabfe193b52d3b
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Device Details

“Rusch” Laryngoflex Tube
TW: “路希”喉頭管
Risk Class 2
MD

Registration Details

d3f125cdf3fb919908aabfe193b52d3b

Ministry of Health Medical Device Import No. 026128

DHA05602612808

Company Information

Germany

Product Details

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

D Devices for anesthesiology

D5800 Trachetomy tube and its balloon

Imported from abroad

Dates and Status

May 01, 2014

May 01, 2024