GUDIDData
eudamed_udi Primary ID: 04260102130043

PALACOS R+G (UDI 04260102130043)

Manufactured by Heraeus Medical GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PALACOS R+G - Primary ID 04260102130043

Device Regulatory Overview

The PALACOS R+G (Model/Catalog Number: 66017750_Legacy) is a medical device manufactured by Heraeus Medical GmbH. This product is indexed under FDA Product Code / Category Classification P099001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
66017750_Legacy
Product Code / EMDN
P099001
Device Name
PALACOS R+G
Database Sync Date
2026-08-09 17:32:26

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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Frequently Asked Questions

Who is the primary manufacturer of PALACOS R+G?

The registered manufacturer of record for PALACOS R+G is Heraeus Medical GmbH.

What is the Primary UDI-DI identifier for PALACOS R+G?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260102130043.

What classification code is assigned to this device?

This device is registered under product classification code P099001.

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