gudid Primary ID: 550661

RINN (UDI 550661)

Manufactured by Dentsply International Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RINN (Model/Catalog Number: 550661) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EHA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 550661
Product Code / EMDN: EHA
Device Name: RINN XCP-ORA For Stickybacks Positioning Kit
Database Sync Date: 2026-08-09 09:02:02

Full Regulatory Attributes

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{
    "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 RINN?

The registered manufacturer of record for RINN is Dentsply International Inc..

What is the Primary UDI-DI identifier for RINN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 550661.

What classification code is assigned to this device?

This device is registered under product classification code EHA.

Similar Classification Devices (EHA)

Other Devices by Dentsply International Inc.

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