gudid
Primary ID: 95701
Mosie Baby Pregnancy Test (UDI 95701)
Manufactured by GERMAINE LABORATORIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mosie Baby Pregnancy Test - Primary ID 95701
Device Regulatory Overview
The Mosie Baby Pregnancy Test (Model/Catalog Number: 95701) is a medical device manufactured by GERMAINE LABORATORIES, INC. This product is indexed under FDA Product Code / Category Classification DHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 95701
- Product Code / EMDN
- DHA
- Device Name
- Urine Midstream, Rapid qualitative test to detect the presence of hCG in urine. Designed for self testing (home). Results within 3 minutes.
- 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 Mosie Baby Pregnancy Test?
The registered manufacturer of record for Mosie Baby Pregnancy Test is GERMAINE LABORATORIES, INC.
What is the Primary UDI-DI identifier for Mosie Baby Pregnancy Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 95701.
What classification code is assigned to this device?
This device is registered under product classification code DHA.
Similar Classification Devices (DHA)
Other Devices by GERMAINE LABORATORIES, INC
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