GUDIDData
eudamed_udi Primary ID: 04250556607482

ergoloc large (UDI 04250556607482)

Manufactured by spektramed GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ergoloc large - Primary ID 04250556607482

Device Regulatory Overview

The ergoloc large (Model/Catalog Number: 8270) is a medical device manufactured by spektramed GmbH. This product is indexed under FDA Product Code / Category Classification Y060303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8270
Product Code / EMDN
Y060303
Device Name
ergoloc
Database Sync Date
2026-08-09 17:19:44

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 ergoloc large?

The registered manufacturer of record for ergoloc large is spektramed GmbH.

What is the Primary UDI-DI identifier for ergoloc large?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250556607482.

What classification code is assigned to this device?

This device is registered under product classification code Y060303.

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