gudid
Primary ID: 1000-C
Reagent Kit (UDI 1000-C)
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 1000-C
Device Regulatory Overview
The Reagent Kit (Model/Catalog Number: 1000-C) 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
- 1000-C
- Product Code / EMDN
- CDF
- Device Name
- HPLC Reagent Kit, VMA, HVA, 5-HIAA in urine
- 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 1000-C.
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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