GUDIDData
eudamed_udi Primary ID: 05052674066344

Delphic V (UDI 05052674066344)

Manufactured by Davis Schottlander & Davis Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Delphic V - Primary ID 05052674066344

Device Regulatory Overview

The Delphic V (Model/Catalog Number: VP:D2:3MU) is a medical device manufactured by Davis Schottlander & Davis Ltd. This product is indexed under FDA Product Code / Category Classification P01020180 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VP:D2:3MU
Product Code / EMDN
P01020180
Device Name
VP:D2:3MU
Database Sync Date
2026-08-09 16:28:47

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of Delphic V?

The registered manufacturer of record for Delphic V is Davis Schottlander & Davis Ltd.

What is the Primary UDI-DI identifier for Delphic V?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05052674066344.

What classification code is assigned to this device?

This device is registered under product classification code P01020180.

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