gudid
Primary ID: 97038
FYI URINE PREGNANCY (UDI 97038)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FYI URINE PREGNANCY - Primary ID 97038
Device Regulatory Overview
The FYI URINE PREGNANCY (Model/Catalog Number: 97038) 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
- 97038
- 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 FYI URINE PREGNANCY?
The registered manufacturer of record for FYI URINE PREGNANCY is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for FYI URINE PREGNANCY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 97038.
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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