Taiwan FDA registration c9fa24941bf57c5f1851fc342df2156f

“OMNIMATE” MANUAL RESUSCITATOR AND ACCESSORIES

TW: “廣鎬”人工呼吸器及其配件

Taiwan·Risk Class 2·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered Nov 27, 2018 – Nov 27, 2028Active

Registration details

Analysis ID: c9fa24941bf57c5f1851fc342df2156f
License Form: Ministry of Health Medical Device Manufacturing No. 006238

Company information

Manufacturer: OMNIMATE ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: OMNIMATE ENTERPRISE CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5915 Manual Emergency Respirator
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 27, 2018
Expiry Date: Nov 27, 2028

About this record

Access comprehensive regulatory information for “OMNIMATE” MANUAL RESUSCITATOR AND ACCESSORIES in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9fa24941bf57c5f1851fc342df2156f and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..

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