gudid
Primary ID: 80800
Reagent Kit (UDI 80800)
Manufactured by Chromsystems Instruments + Chemicals GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reagent Kit - Primary ID 80800
Device Regulatory Overview
The Reagent Kit (Model/Catalog Number: 80800) is a medical device manufactured by Chromsystems Instruments + Chemicals GmbH. This product is indexed under FDA Product Code / Category Classification CDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80800
- Product Code / EMDN
- CDF
- Device Name
- MassChrom Biogenic Amines/Metabolites in urine, Sample Prep Set VMA, HVA, 5-HIAA including autosampler vials
- 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 Reagent Kit?
The registered manufacturer of record for Reagent Kit is Chromsystems Instruments + Chemicals GmbH.
What is the Primary UDI-DI identifier for Reagent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80800.
What classification code is assigned to this device?
This device is registered under product classification code CDF.
Similar Classification Devices (CDF)
Other Devices by Chromsystems Instruments + Chemicals GmbH
Programmatic Export
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JSON API Endpoint