gudid
Primary ID: 41125
AIMSCREEN AMP (UDI 41125)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSCREEN AMP - Primary ID 41125
Device Regulatory Overview
The AIMSCREEN AMP (Model/Catalog Number: 41125) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification DKZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 41125
- Product Code / EMDN
- DKZ
- Device Name
- Lateral flow immunoassay for the detection of Amphetamine (AMP) 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 AMP?
The registered manufacturer of record for AIMSCREEN AMP is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSCREEN AMP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 41125.
What classification code is assigned to this device?
This device is registered under product classification code DKZ.
Similar Classification Devices (DKZ)
Other Devices by GERMAINE LABORATORIES, INC
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