GUDIDData
eudamed_udi Primary ID: 04050674064439

ROTANTA 460 Robotic, 110-120V 50-60Hz (UDI 04050674064439)

Manufactured by Andreas Hettich GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ROTANTA 460 Robotic, 110-120V 50-60Hz - Primary ID 04050674064439

Device Regulatory Overview

The ROTANTA 460 Robotic, 110-120V 50-60Hz (Model/Catalog Number: 5680-71) is a medical device manufactured by Andreas Hettich GmbH. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5680-71
Product Code / EMDN
W02069005
Device Name
ROTANTA 460 Robotic
Database Sync Date
2026-08-09 16:28:56

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 ROTANTA 460 Robotic, 110-120V 50-60Hz?

The registered manufacturer of record for ROTANTA 460 Robotic, 110-120V 50-60Hz is Andreas Hettich GmbH.

What is the Primary UDI-DI identifier for ROTANTA 460 Robotic, 110-120V 50-60Hz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050674064439.

What classification code is assigned to this device?

This device is registered under product classification code W02069005.

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