Taiwan FDA registration 54467ab45f901d9f39913c0c12d188cf
"OMNIMATE" Anesthesia breathing circuit (Non-Sterile)
TW: "廣鎬" 麻醉呼吸管路 (未滅菌)
Taiwan·Risk Class 1·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered Sep 02, 2020 – Sep 02, 2025ExpiredRegistration details
- Analysis ID
- 54467ab45f901d9f39913c0c12d188cf
- License Form
- Ministry of Health Medical Device Manufacturing No. 008577
Company information
- Manufacturer
- OMNIMATE ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- OMNIMATE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "anesthesia breathing circuit (D.5240)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5240 Anesthesia breathing line
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 02, 2020
- Expiry Date
- Sep 02, 2025
About this record
Access comprehensive regulatory information for "OMNIMATE" Anesthesia breathing circuit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 54467ab45f901d9f39913c0c12d188cf and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..
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