gudid Primary ID: R+G

PALACOS (UDI R+G)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

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

Technical Specifications

Model Number: R+G
Product Code / EMDN: MBB
Device Name: PALACOS R+G is a fast setting polymer containing gentamicin, for use in bone surgery. Mixing of the two component system, consisting of a powder and a liquid, initially produces a liquid and then a paste, which is used to anchor the prosthesis to the bone. The hardened bone cement allows stable fixation of the prosthesis and Transfers all stresses produced in a movement to the bone via the large interface. Insoluble zirconium dioxide is included in the cement powder as an X ray contrast medium. The chlorophyll additive serves as optical marking of the bone cement at the site of the operation.
Database Sync Date: 2026-08-09 09:09:40

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?

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

What is the Primary UDI-DI identifier for PALACOS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R+G.

What classification code is assigned to this device?

This device is registered under product classification code MBB.

Similar Classification Devices (MBB)

Other Devices by Heraeus Medical GmbH

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