Taiwan FDA registration 71357e8df1f4256b03ee1f426f47b80d
“OMNIMATE” Obstetric-gynecologic general manual instrument (Non-Sterile)
TW: “廣鎬”婦產科用一般手動器械 (未滅菌)
Taiwan·Risk Class 1·MD·OMNIMATE ENTERPRISE CO., LTD.·Registered Feb 22, 2018 – Feb 22, 2028ActiveRegistration details
- Analysis ID
- 71357e8df1f4256b03ee1f426f47b80d
- License Form
- Ministry of Health Medical Device Manufacturing No. 007125
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 scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L4520 General manual instruments for obstetrics and gynecology
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 22, 2018
- Expiry Date
- Feb 22, 2028
About this record
Access comprehensive regulatory information for “OMNIMATE” Obstetric-gynecologic general manual instrument (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 71357e8df1f4256b03ee1f426f47b80d and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is OMNIMATE ENTERPRISE CO., LTD..
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