gudid
Primary ID: 00683
STA - Heparin Control (UDI 00683)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STA - Heparin Control - Primary ID 00683
Device Regulatory Overview
The STA - Heparin Control (Model/Catalog Number: 00683) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification KFF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00683
- Product Code / EMDN
- KFF
- 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 - Heparin Control?
The registered manufacturer of record for STA - Heparin Control is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for STA - Heparin Control?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00683.
What classification code is assigned to this device?
This device is registered under product classification code KFF.
Similar Classification Devices (KFF)
Other Devices by DIAGNOSTICA STAGO
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