GUDIDData
gudid Primary ID: 28007

Plasma Calibration Standard (UDI 28007)

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 Calibration Standard - Primary ID 28007

Device Regulatory Overview

The Plasma Calibration Standard (Model/Catalog Number: 28007) 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
28007
Product Code / EMDN
JIX
Device Name
Plasma Calibration Standard Perazine, Quetiapine, Citalopram
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Plasma Calibration Standard?

The registered manufacturer of record for Plasma Calibration Standard is Chromsystems Instruments + Chemicals GmbH.

What is the Primary UDI-DI identifier for Plasma Calibration Standard?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28007.

What classification code is assigned to this device?

This device is registered under product classification code JIX.

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