gudid
Primary ID: 49425
AIMSCREEN OXY (UDI 49425)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSCREEN OXY - Primary ID 49425
Device Regulatory Overview
The AIMSCREEN OXY (Model/Catalog Number: 49425) 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
- 49425
- Product Code / EMDN
- DJG
- Device Name
- Lateral flow immunoassay for the detection of Oxycodone (OXY) in urine.
- Database Sync Date
- 2026-08-09 09:04:20
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 AIMSCREEN OXY?
The registered manufacturer of record for AIMSCREEN OXY is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSCREEN OXY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 49425.
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
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