GUDIDData
gudid Primary ID: 92025/XT

Plasma Calibrator Set (UDI 92025/XT)

Manufactured by Chromsystems Instruments + Chemicals GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Plasma Calibrator Set - Primary ID 92025/XT

Device Regulatory Overview

The Plasma Calibrator Set (Model/Catalog Number: 92025/XT) 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/XT
Product Code / EMDN
JIX
Device Name
3PLUS1 Multilevel Plasma Calibrator Set MassTox Antiepileptic Drugs/EXTENDED
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/XT.

What classification code is assigned to this device?

This device is registered under product classification code JIX.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint