GUDIDData
gudid Primary ID: 1700439-001

Set iChiropro (UDI 1700439-001)

Manufactured by Bien-Air Dental SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Set iChiropro - Primary ID 1700439-001

Device Regulatory Overview

The Set iChiropro (Model/Catalog Number: 1700439-001) is a medical device manufactured by Bien-Air Dental SA. This product is indexed under FDA Product Code / Category Classification EBW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1700439-001
Product Code / EMDN
EBW
Device Name
Sets of iChiropro systems and their dental micromotors or contra-angles plus relevant accessories
Database Sync Date
2026-08-09 09:09:45

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 Set iChiropro?

The registered manufacturer of record for Set iChiropro is Bien-Air Dental SA.

What is the Primary UDI-DI identifier for Set iChiropro?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1700439-001.

What classification code is assigned to this device?

This device is registered under product classification code EBW.

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