gudid
Primary ID: 100000
RIVA (UDI 100000)
Manufactured by ARxIUM Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIVA - Primary ID 100000
Device Regulatory Overview
The RIVA (Model/Catalog Number: 100000) is a medical device manufactured by ARxIUM Inc. This product is indexed under FDA Product Code / Category Classification NEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100000
- Product Code / EMDN
- NEP
- Device Name
- A device used to prepare IV bags and syringes for hospital and compounding pharmacies.
- Database Sync Date
- 2026-08-09 09:04:20
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 RIVA?
The registered manufacturer of record for RIVA is ARxIUM Inc.
What is the Primary UDI-DI identifier for RIVA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100000.
What classification code is assigned to this device?
This device is registered under product classification code NEP.
Similar Classification Devices (NEP)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint