Plasma Calibrator Set (UDI 92025-XT2)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Device Regulatory Overview
The Plasma Calibrator Set (Model/Catalog Number: 92025-XT2) is a medical device manufactured by Chromsystems Instruments + Chemicals GmbH. This product is indexed under FDA Product Code / Category Classification JIX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 92025-XT2
- Product Code / EMDN
- JIX
- Device Name
- 3PLUS1 Multilevel Plasma Calibrator Set MassTox Antiepileptic Drugs XT2
- Database Sync Date
- 2026-08-09 09:11:40
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 Plasma Calibrator Set?
The registered manufacturer of record for Plasma Calibrator Set is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Plasma Calibrator Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 92025-XT2.
What classification code is assigned to this device?
This device is registered under product classification code JIX.
Similar Classification Devices (JIX)
Other Devices by Chromsystems Instruments + Chemicals GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint