gudid
Primary ID: 00723
STA - Deficient XI (UDI 00723)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STA - Deficient XI - Primary ID 00723
Device Regulatory Overview
The STA - Deficient XI (Model/Catalog Number: 00723) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification GJT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00723
- Product Code / EMDN
- GJT
- Device Name
- Database Sync Date
- 2026-08-09 09:48:33
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 - Deficient XI?
The registered manufacturer of record for STA - Deficient XI is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for STA - Deficient XI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00723.
What classification code is assigned to this device?
This device is registered under product classification code GJT.
Similar Classification Devices (GJT)
Other Devices by DIAGNOSTICA STAGO
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