GUDIDData
gudid Primary ID: BP3NG1-1AMFT(2878064)

Foster & Thrive (UDI BP3NG1-1AMFT(2878064))

Manufactured by MCKESSON CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Foster & Thrive - Primary ID BP3NG1-1AMFT(2878064)

Device Regulatory Overview

The Foster & Thrive (Model/Catalog Number: BP3NG1-1AMFT(2878064)) is a medical device manufactured by MCKESSON CORPORATION. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BP3NG1-1AMFT(2878064)
Product Code / EMDN
DXN
Device Name
Database Sync Date
2026-08-09 09:00:34

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Foster & Thrive?

The registered manufacturer of record for Foster & Thrive is MCKESSON CORPORATION.

What is the Primary UDI-DI identifier for Foster & Thrive?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BP3NG1-1AMFT(2878064).

What classification code is assigned to this device?

This device is registered under product classification code DXN.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint