Taiwan FDA registration 556f123664cb47330f3f821bc2cbf209
“OMNIMATE” TRACHEAL TUBE
TW: “廣鎬”氣管內管
Taiwan·Risk Class 2·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered Oct 18, 2018 – Oct 18, 2028ActiveRegistration details
- Analysis ID
- 556f123664cb47330f3f821bc2cbf209
- License Form
- Ministry of Health Medical Device Manufacturing No. 006218
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)
- D5730 Endotracheal tube
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 18, 2018
- Expiry Date
- Oct 18, 2028
About this record
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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