Calibration Standard (UDI 6003)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Device Regulatory Overview
The Calibration Standard (Model/Catalog Number: 6003) 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
- 6003
- Product Code / EMDN
- JIX
- Device Name
- Calibration Standard Catecholamines
- 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 Calibration Standard?
The registered manufacturer of record for Calibration Standard is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Calibration Standard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6003.
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