gudid
Primary ID: ST10M5S8C
BiDop 7 probe (UDI ST10M5S8C)
Manufactured by KOVEN TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BiDop 7 probe - Primary ID ST10M5S8C
Device Regulatory Overview
The BiDop 7 probe (Model/Catalog Number: ST10M5S8C) is a medical device manufactured by KOVEN TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification DPW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ST10M5S8C
- Product Code / EMDN
- DPW
- Device Name
- 10 mhz curly cable Probe for Bidop 7
- Database Sync Date
- 2026-08-09 09:46:58
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 BiDop 7 probe?
The registered manufacturer of record for BiDop 7 probe is KOVEN TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for BiDop 7 probe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ST10M5S8C.
What classification code is assigned to this device?
This device is registered under product classification code DPW.
Similar Classification Devices (DPW)
Other Devices by KOVEN TECHNOLOGY, INC.
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