gudid
Primary ID: V8
STA Coag Expert (UDI V8)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STA Coag Expert - Primary ID V8
Device Regulatory Overview
The STA Coag Expert (Model/Catalog Number: V8) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification JQP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V8
- Product Code / EMDN
- JQP
- Device Name
- Database Sync Date
- 2026-08-09 09:23:29
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 STA Coag Expert?
The registered manufacturer of record for STA Coag Expert is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for STA Coag Expert?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V8.
What classification code is assigned to this device?
This device is registered under product classification code JQP.
Similar Classification Devices (JQP)
Other Devices by DIAGNOSTICA STAGO
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