Precolumn Cartridge (UDI 15012)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Device Regulatory Overview
The Precolumn Cartridge (Model/Catalog Number: 15012) is a medical device manufactured by Chromsystems Instruments + Chemicals GmbH. This product is indexed under FDA Product Code / Category Classification KZR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 15012
- Product Code / EMDN
- KZR
- Device Name
- PEEK-encased Prefilter
- Database Sync Date
- 2026-08-09 09:11:40
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Precolumn Cartridge?
The registered manufacturer of record for Precolumn Cartridge is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Precolumn Cartridge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15012.
What classification code is assigned to this device?
This device is registered under product classification code KZR.
Similar Classification Devices (KZR)
Other Devices by Chromsystems Instruments + Chemicals GmbH
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