GUDIDData
eudamed_udi Primary ID: 08435566609763

RA Shank Ratchet adapter accessory (UDI 08435566609763)

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 RA Shank Ratchet adapter accessory - Primary ID 08435566609763

Device Regulatory Overview

The RA Shank Ratchet adapter accessory (Model/Catalog Number: IPD/DI-KA-91) 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/DI-KA-91
Product Code / EMDN
Q010280
Device Name
Screwdriver
Database Sync Date
2026-08-09 16:28:59

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 RA Shank Ratchet adapter accessory?

The registered manufacturer of record for RA Shank Ratchet adapter accessory is IMPLANT PROTESIS DENTAL 2004 S.L..

What is the Primary UDI-DI identifier for RA Shank Ratchet adapter accessory?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435566609763.

What classification code is assigned to this device?

This device is registered under product classification code Q010280.

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