gudid
Primary ID: 57016
Prefilter (UDI 57016)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prefilter - Primary ID 57016
Device Regulatory Overview
The Prefilter (Model/Catalog Number: 57016) is a medical device manufactured by Chromsystems Instruments + Chemicals GmbH. This product is indexed under FDA Product Code / Category Classification LXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 57016
- Product Code / EMDN
- LXG
- Device Name
- PEEK Prefilter 2 m, MassScreen Amino Acids, Acylcarnitines EXTENDED (non-derivatised)
- 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 Prefilter?
The registered manufacturer of record for Prefilter is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Prefilter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 57016.
What classification code is assigned to this device?
This device is registered under product classification code LXG.
Similar Classification Devices (LXG)
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