gudid
Primary ID: BT5M05S8A
BT5M05S8A (UDI BT5M05S8A)
Manufactured by KOVEN TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BT5M05S8A - Primary ID BT5M05S8A
Device Regulatory Overview
The BT5M05S8A (Model/Catalog Number: BT5M05S8A) is a medical device manufactured by KOVEN TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification JOP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BT5M05S8A
- Product Code / EMDN
- JOP
- Device Name
- 5 MHz straight cable clinic CW Doppler probe.
- 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 BT5M05S8A?
The registered manufacturer of record for BT5M05S8A is KOVEN TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for BT5M05S8A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BT5M05S8A.
What classification code is assigned to this device?
This device is registered under product classification code JOP.
Similar Classification Devices (JOP)
Other Devices by KOVEN TECHNOLOGY, INC.
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