gudid
Primary ID: MV pro 40
PALACOS (UDI MV pro 40)
Manufactured by Heraeus Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PALACOS - Primary ID MV pro 40
Device Regulatory Overview
The PALACOS (Model/Catalog Number: MV pro 40) is a medical device manufactured by Heraeus Medical GmbH. This product is indexed under FDA Product Code / Category Classification LOD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MV pro 40
- Product Code / EMDN
- LOD
- Device Name
- The PALACOS MV pro system consists of a mixing and application system prefilled with PALACOS polymer powder and monomer liquid. PALACOS MV pro is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.
- Database Sync Date
- 2026-08-09 09:17:36
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)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 MV pro 40.
What classification code is assigned to this device?
This device is registered under product classification code LOD.
Similar Classification Devices (LOD)
Other Devices by Heraeus Medical GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint