UltraMint Pro (UDI 06972597780112)
Manufactured by Changzhou Sifary Medical Technology Co., Ltd.
Device Regulatory Overview
The UltraMint Pro (Model/Catalog Number: 6680001) is a medical device manufactured by Changzhou Sifary Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L159009 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6680001
- Product Code / EMDN
- L159009
- Device Name
- UltraMint Pro
- Database Sync Date
- 2026-08-09 16:46:16
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of UltraMint Pro?
The registered manufacturer of record for UltraMint Pro is Changzhou Sifary Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for UltraMint Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972597780112.
What classification code is assigned to this device?
This device is registered under product classification code L159009.
Similar Classification Devices (L159009)
Other Devices by Changzhou Sifary Medical Technology Co., Ltd.
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