gudid
Primary ID: BP3GK1-3FRA
RITE AID (UDI BP3GK1-3FRA)
Manufactured by MICROLIFE USA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RITE AID - Primary ID BP3GK1-3FRA
Device Regulatory Overview
The RITE AID (Model/Catalog Number: BP3GK1-3FRA) is a medical device manufactured by MICROLIFE USA, INC.. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BP3GK1-3FRA
- Product Code / EMDN
- DXN
- Device Name
- Database Sync Date
- 2026-08-09 09:00:34
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 RITE AID?
The registered manufacturer of record for RITE AID is MICROLIFE USA, INC..
What is the Primary UDI-DI identifier for RITE AID?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BP3GK1-3FRA.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by MICROLIFE USA, INC.
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