ST2305 (UDI 06972820961134)
Manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.
Device Regulatory Overview
The ST2305 (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 V03010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07-10-00
- Product Code / EMDN
- V03010201
- Device Name
- Temperature Probe
- Database Sync Date
- 2026-08-09 18:13:55
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 ST2305?
The registered manufacturer of record for ST2305 is Shenzhen SINO-K Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for ST2305?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972820961134.
What classification code is assigned to this device?
This device is registered under product classification code V03010201.
Similar Classification Devices (V03010201)
Other Devices by Shenzhen SINO-K Medical Technology Co., Ltd.
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