eudamed_udi
Primary ID: 05060596025820
ACTIVE ERA (UDI 05060596025820)
Manufactured by One Retail Group Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACTIVE ERA - Primary ID 05060596025820
Device Regulatory Overview
The ACTIVE ERA (Model/Catalog Number: AE-FA-03R-EU) is a medical device manufactured by One Retail Group Limited. This product is indexed under FDA Product Code / Category Classification Y0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AE-FA-03R-EU
- Product Code / EMDN
- Y0999
- Device Name
- Active Era First Aid Kit 320 pcs – Red
- Database Sync Date
- 2026-08-09 16:30:40
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 ACTIVE ERA?
The registered manufacturer of record for ACTIVE ERA is One Retail Group Limited.
What is the Primary UDI-DI identifier for ACTIVE ERA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060596025820.
What classification code is assigned to this device?
This device is registered under product classification code Y0999.
Similar Classification Devices (Y0999)
Other Devices by One Retail Group Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint