gudid
Primary ID: CRP-20H1N
CRP Probe (UDI CRP-20H1N)
Manufactured by KOVEN TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CRP Probe - Primary ID CRP-20H1N
Device Regulatory Overview
The CRP Probe (Model/Catalog Number: CRP-20H1N) is a medical device manufactured by KOVEN TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CRP-20H1N
- Product Code / EMDN
- JAF
- Device Name
- 1.2mm tip PW cardiovascular Doppler probe, 20 MHz
- 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 CRP Probe?
The registered manufacturer of record for CRP Probe is KOVEN TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for CRP Probe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CRP-20H1N.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
Other Devices by KOVEN TECHNOLOGY, INC.
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