gudid
Primary ID: 00950
Asserachrom -TG (UDI 00950)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Asserachrom -TG - Primary ID 00950
Device Regulatory Overview
The Asserachrom -TG (Model/Catalog Number: 00950) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification JBX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00950
- Product Code / EMDN
- JBX
- Device Name
- Database Sync Date
- 2026-08-09 09:23:29
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Asserachrom -TG?
The registered manufacturer of record for Asserachrom -TG is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for Asserachrom -TG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00950.
What classification code is assigned to this device?
This device is registered under product classification code JBX.
Similar Classification Devices (JBX)
Other Devices by DIAGNOSTICA STAGO
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint