GUDIDData
eudamed_udi Primary ID: 08435566627774

Temporary abutment Non-Engaging RP (UDI 08435566627774)

Manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Temporary abutment Non-Engaging RP - Primary ID 08435566627774

Device Regulatory Overview

The Temporary abutment Non-Engaging RP (Model/Catalog Number: IPD/2A-PR-07) is a medical device manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.. This product is indexed under FDA Product Code / Category Classification Q01020605 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IPD/2A-PR-07
Product Code / EMDN
Q01020605
Device Name
Cementing abutment ; Temporary abutment
Database Sync Date
2026-08-09 16:29:58

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 Temporary abutment Non-Engaging RP?

The registered manufacturer of record for Temporary abutment Non-Engaging RP is IMPLANT PROTESIS DENTAL 2004 S.L..

What is the Primary UDI-DI identifier for Temporary abutment Non-Engaging RP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435566627774.

What classification code is assigned to this device?

This device is registered under product classification code Q01020605.

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