GUDIDData
eudamed_udi Primary ID: 08050323061167

PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT (UDI 08050323061167)

Manufactured by Permedica S.p.A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT - Primary ID 08050323061167

Device Regulatory Overview

The PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT (Model/Catalog Number: S19021) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification V06010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S19021
Product Code / EMDN
V06010101
Device Name
Trial Component
Database Sync Date
2026-08-09 16:45:08

Full Regulatory Attributes

🔒 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 PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT?

The registered manufacturer of record for PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT is Permedica S.p.A.

What is the Primary UDI-DI identifier for PM ProMotion: Trial Prosthesis Neck Lateralized - SHORT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323061167.

What classification code is assigned to this device?

This device is registered under product classification code V06010101.

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