GUDIDData
eudamed_udi Primary ID: 05060481691260

SG110 Twin Axis Electrogoniometer (UDI 05060481691260)

Manufactured by Biometrics Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SG110 Twin Axis Electrogoniometer - Primary ID 05060481691260

Device Regulatory Overview

The SG110 Twin Axis Electrogoniometer (Model/Catalog Number: SG110) is a medical device manufactured by Biometrics Ltd. This product is indexed under FDA Product Code / Category Classification V030202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SG110
Product Code / EMDN
V030202
Device Name
Data Acquisition Products
Database Sync Date
2026-08-09 16:48:37

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 SG110 Twin Axis Electrogoniometer?

The registered manufacturer of record for SG110 Twin Axis Electrogoniometer is Biometrics Ltd.

What is the Primary UDI-DI identifier for SG110 Twin Axis Electrogoniometer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060481691260.

What classification code is assigned to this device?

This device is registered under product classification code V030202.

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