gudid Primary ID: Nozzle Slim

PALAMIX (UDI Nozzle Slim)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PALAMIX (Model/Catalog Number: Nozzle Slim) is a medical device manufactured by Heraeus Medical GmbH. This product is indexed under FDA Product Code / Category Classification KIH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Nozzle Slim
Product Code / EMDN: KIH
Device Name: PALAMIX nozzles are available in different lengths and diameters for applying bone cement pre-mixed by the PALAMIX uno or PALAMIX duo vacuum mixing system. PALAMIX nozzle slim is the accessory of PALAMIX uno or PALAMIX duo vacuum mixing system intended for use in placing bone cement into surgical sites.
Database Sync Date: 2026-08-09 09:17:36

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 PALAMIX?

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

What is the Primary UDI-DI identifier for PALAMIX?

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

What classification code is assigned to this device?

This device is registered under product classification code KIH.

Similar Classification Devices (KIH)

Other Devices by Heraeus Medical GmbH

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