gudid
Primary ID: BXI-113-25-02
BioStrip P (UDI BXI-113-25-02)
Manufactured by PRINCETON BIOMEDITECH CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioStrip P - Primary ID BXI-113-25-02
Device Regulatory Overview
The BioStrip P (Model/Catalog Number: BXI-113-25-02) is a medical device manufactured by PRINCETON BIOMEDITECH CORPORATION. This product is indexed under FDA Product Code / Category Classification DHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BXI-113-25-02
- Product Code / EMDN
- DHA
- Device Name
- BioStrip P; 25 Test kit; CE (for LifeSign)
- Database Sync Date
- 2026-08-09 10:00:19
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 BioStrip P?
The registered manufacturer of record for BioStrip P is PRINCETON BIOMEDITECH CORPORATION.
What is the Primary UDI-DI identifier for BioStrip P?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BXI-113-25-02.
What classification code is assigned to this device?
This device is registered under product classification code DHA.
Similar Classification Devices (DHA)
Other Devices by PRINCETON BIOMEDITECH CORPORATION
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