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“OMNIMATE” TRACHEAL TUBE - Taiwan Registration 556f123664cb47330f3f821bc2cbf209

Access comprehensive regulatory information for “OMNIMATE” TRACHEAL TUBE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 556f123664cb47330f3f821bc2cbf209 and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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556f123664cb47330f3f821bc2cbf209
Registration Details
Taiwan FDA Registration: 556f123664cb47330f3f821bc2cbf209
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Device Details

“OMNIMATE” TRACHEAL TUBE
TW: “廣鎬”氣管內管
Risk Class 2
MD

Registration Details

556f123664cb47330f3f821bc2cbf209

Ministry of Health Medical Device Manufacturing No. 006218

Company Information

Taiwan, Province of China

Product Details

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

D Devices for anesthesiology

D5730 Endotracheal tube

Produced in Taiwan, China

Dates and Status

Oct 18, 2018

Oct 18, 2028