gudid
Primary ID: 48125
AIMSCREEN MOP (UDI 48125)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSCREEN MOP - Primary ID 48125
Device Regulatory Overview
The AIMSCREEN MOP (Model/Catalog Number: 48125) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification DJG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 48125
- Product Code / EMDN
- DJG
- Device Name
- Lateral flow immunoassay for the detection of Opiate (OPI) in urine.
- 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 AIMSCREEN MOP?
The registered manufacturer of record for AIMSCREEN MOP is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSCREEN MOP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48125.
What classification code is assigned to this device?
This device is registered under product classification code DJG.
Similar Classification Devices (DJG)
Other Devices by GERMAINE LABORATORIES, INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint