GUDIDData
gudid Primary ID: CH2

ACCESS (UDI CH2)

Manufactured by RELIANCE ORTHODONTIC PRODUCTS INC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACCESS - Primary ID CH2

Device Regulatory Overview

The ACCESS (Model/Catalog Number: CH2) is a medical device manufactured by RELIANCE ORTHODONTIC PRODUCTS INC. This product is indexed under FDA Product Code / Category Classification EIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CH2
Product Code / EMDN
EIF
Device Name
The ACCESS Cheek Retractors are intended for use in pulling the cheeks back from the buccal and labial surfaces of the teeth during orthodontic procedures. Pediatric Size - Special posterior pads comfortably hold the cheeks away and allow excellent "accessibility" to the bicuspid and molar area. Spring stainless steel bow allows for adjustment and pivot points provide greater comfort.
Database Sync Date
2026-08-09 09:05:50

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 ACCESS?

The registered manufacturer of record for ACCESS is RELIANCE ORTHODONTIC PRODUCTS INC.

What is the Primary UDI-DI identifier for ACCESS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CH2.

What classification code is assigned to this device?

This device is registered under product classification code EIF.

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