GUDIDData
eudamed_udi Primary ID: 08052275307973

PANTHEON PHR (UDI 08052275307973)

Manufactured by Adler Ortho S.p.A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PANTHEON PHR - Primary ID 08052275307973

Device Regulatory Overview

The PANTHEON PHR (Model/Catalog Number: 2800630) is a medical device manufactured by Adler Ortho S.p.A. This product is indexed under FDA Product Code / Category Classification P09010303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2800630
Product Code / EMDN
P09010303
Device Name
PANTHEON GLENOSPHERE D. 32 OFFSET +8
Database Sync Date
2026-08-09 18:44:46

Full Regulatory Attributes

πŸ”’ 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 PANTHEON PHR?

The registered manufacturer of record for PANTHEON PHR is Adler Ortho S.p.A.

What is the Primary UDI-DI identifier for PANTHEON PHR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052275307973.

What classification code is assigned to this device?

This device is registered under product classification code P09010303.

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