GUDIDData
eudamed_udi Primary ID: 04751040972760

Acupressure Octopus Thoracic-shoulder orthosis (UDI 04751040972760)

Manufactured by AGM orthopaedics

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acupressure Octopus Thoracic-shoulder orthosis - Primary ID 04751040972760

Device Regulatory Overview

The Acupressure Octopus Thoracic-shoulder orthosis (Model/Catalog Number: 100TC0202N) is a medical device manufactured by AGM orthopaedics. This product is indexed under FDA Product Code / Category Classification Y060307 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
100TC0202N
Product Code / EMDN
Y060307
Device Name
Acupressure Octopus spinal orthosis
Database Sync Date
2026-08-09 17:03:26

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 Acupressure Octopus Thoracic-shoulder orthosis?

The registered manufacturer of record for Acupressure Octopus Thoracic-shoulder orthosis is AGM orthopaedics.

What is the Primary UDI-DI identifier for Acupressure Octopus Thoracic-shoulder orthosis?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04751040972760.

What classification code is assigned to this device?

This device is registered under product classification code Y060307.

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