GUDIDData
eudamed_udi Primary ID: 08435566625640

Ti Screw TiN (UDI 08435566625640)

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 Ti Screw TiN - Primary ID 08435566625640

Device Regulatory Overview

The Ti Screw TiN (Model/Catalog Number: IPD/XA-TR-03/TIN) is a medical device manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IPD/XA-TR-03/TIN
Product Code / EMDN
Q010280
Device Name
TIN screws
Database Sync Date
2026-08-09 16:29:08

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 Ti Screw TiN?

The registered manufacturer of record for Ti Screw TiN is IMPLANT PROTESIS DENTAL 2004 S.L..

What is the Primary UDI-DI identifier for Ti Screw TiN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435566625640.

What classification code is assigned to this device?

This device is registered under product classification code Q010280.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint