GUDIDData
eudamed_udi Primary ID: 00884838121133

Standard ECG 3.0 Cable AAMI (UDI 00884838121133)

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 Standard ECG 3.0 Cable AAMI - Primary ID 00884838121133

Device Regulatory Overview

The Standard ECG 3.0 Cable AAMI (Model/Catalog Number: 989803193731) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1203020299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
989803193731
Product Code / EMDN
Z1203020299
Device Name
Reusable Electrocardiographic Leads
Database Sync Date
2026-08-09 16:50:33

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 Standard ECG 3.0 Cable AAMI?

The registered manufacturer of record for Standard ECG 3.0 Cable AAMI is Philips Medizin Systeme Böblingen GmbH.

What is the Primary UDI-DI identifier for Standard ECG 3.0 Cable AAMI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838121133.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020299.

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