GUDIDData
eudamed_udi Primary ID: 00884838093218

Avalon Toco MP Transducer (UDI 00884838093218)

Manufactured by Philips Medizin Systeme Böblingen GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avalon Toco MP Transducer - Primary ID 00884838093218

Device Regulatory Overview

The Avalon Toco MP Transducer (Model/Catalog Number: 867248) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1208010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
867248
Product Code / EMDN
Z1208010499
Device Name
Avalon Toco MP Transducer
Database Sync Date
2026-08-09 16:46:14

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 Avalon Toco MP Transducer?

The registered manufacturer of record for Avalon Toco MP Transducer is Philips Medizin Systeme Böblingen GmbH.

What is the Primary UDI-DI identifier for Avalon Toco MP Transducer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838093218.

What classification code is assigned to this device?

This device is registered under product classification code Z1208010499.

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