gudid Primary ID: 540927

RINN (UDI 540927)

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: 540927) 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: 540927
Product Code / EMDN: EHA
Device Name: RINN XCP/BAI Bite-Wing Arm
Database Sync Date: 2026-08-09 09:02:02

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 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 540927.

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.

Programmatic Export

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

JSON API Endpoint