GUDIDData
eudamed_udi Primary ID: 08050323060450

PBF Stem: Trial Cone for Mark S Rasps - Size 01-0 (UDI 08050323060450)

Manufactured by Permedica S.p.A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PBF Stem: Trial Cone for Mark S Rasps - Size 01-0 - Primary ID 08050323060450

Device Regulatory Overview

The PBF Stem: Trial Cone for Mark S Rasps - Size 01-0 (Model/Catalog Number: S12380) 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
S12380
Product Code / EMDN
V06010101
Device Name
Trial Component
Database Sync Date
2026-08-09 16:49:19

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 PBF Stem: Trial Cone for Mark S Rasps - Size 01-0?

The registered manufacturer of record for PBF Stem: Trial Cone for Mark S Rasps - Size 01-0 is Permedica S.p.A.

What is the Primary UDI-DI identifier for PBF Stem: Trial Cone for Mark S Rasps - Size 01-0?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323060450.

What classification code is assigned to this device?

This device is registered under product classification code V06010101.

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