SP7119A (UDI 06972820960588)
Manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.
Device Regulatory Overview
The SP7119A (Model/Catalog Number: 07-10-00) is a medical device manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification C900301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07-10-00
- Product Code / EMDN
- C900301
- Device Name
- SP7119A
- Database Sync Date
- 2026-08-09 17:15:11
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 SP7119A?
The registered manufacturer of record for SP7119A is Shenzhen SINO-K Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for SP7119A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972820960588.
What classification code is assigned to this device?
This device is registered under product classification code C900301.
Similar Classification Devices (C900301)
Other Devices by Shenzhen SINO-K Medical Technology Co., Ltd.
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