gudid
Primary ID: 78103
AIMSTRIP HEMOGLOBIN CONTROL SET (UDI 78103)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSTRIP HEMOGLOBIN CONTROL SET - Primary ID 78103
Device Regulatory Overview
The AIMSTRIP HEMOGLOBIN CONTROL SET (Model/Catalog Number: 78103) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 78103
- Product Code / EMDN
- GGM
- Device Name
- Intended to validate hemoglobin testing using the AimStrip HB Hemoglobin Testing System.
- 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 AIMSTRIP HEMOGLOBIN CONTROL SET?
The registered manufacturer of record for AIMSTRIP HEMOGLOBIN CONTROL SET is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSTRIP HEMOGLOBIN CONTROL SET?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 78103.
What classification code is assigned to this device?
This device is registered under product classification code GGM.
Similar Classification Devices (GGM)
Other Devices by GERMAINE LABORATORIES, INC
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