GUDIDData
eudamed_udi Primary ID: 00884838034228

Avalon CL Basestation (UDI 00884838034228)

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 CL Basestation - Primary ID 00884838034228

Device Regulatory Overview

The Avalon CL Basestation (Model/Catalog Number: 866074) 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
866074
Product Code / EMDN
Z1208010499
Device Name
Fetal Basestation
Database Sync Date
2026-08-09 17:29:54

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 CL Basestation?

The registered manufacturer of record for Avalon CL Basestation is Philips Medizin Systeme Böblingen GmbH.

What is the Primary UDI-DI identifier for Avalon CL Basestation?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838034228.

What classification code is assigned to this device?

This device is registered under product classification code Z1208010499.

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