gudid
Primary ID: 97025
AIMSTEP PREGNANCY (UDI 97025)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIMSTEP PREGNANCY - Primary ID 97025
Device Regulatory Overview
The AIMSTEP PREGNANCY (Model/Catalog Number: 97025) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification JHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 97025
- Product Code / EMDN
- JHI
- Device Name
- Urine cassette test. For the rapid qualitative determination of human Chorionic Gonadotropin (hCG) 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 AIMSTEP PREGNANCY?
The registered manufacturer of record for AIMSTEP PREGNANCY is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for AIMSTEP PREGNANCY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 97025.
What classification code is assigned to this device?
This device is registered under product classification code JHI.
Similar Classification Devices (JHI)
Other Devices by GERMAINE LABORATORIES, INC
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