GUDIDData
eudamed_udi Primary ID: 00884838067868

Transducer C6-2, Variant 1 (UDI 00884838067868)

Manufactured by Philips Ultrasound LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transducer C6-2, Variant 1 - Primary ID 00884838067868

Device Regulatory Overview

The Transducer C6-2, Variant 1 (Model/Catalog Number: 989605418982) is a medical device manufactured by Philips Ultrasound LLC. This product is indexed under FDA Product Code / Category Classification Z110402010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
989605418982
Product Code / EMDN
Z110402010201
Device Name
Non-Invasive Transducers
Database Sync Date
2026-08-09 16:47:14

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 Transducer C6-2, Variant 1?

The registered manufacturer of record for Transducer C6-2, Variant 1 is Philips Ultrasound LLC.

What is the Primary UDI-DI identifier for Transducer C6-2, Variant 1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838067868.

What classification code is assigned to this device?

This device is registered under product classification code Z110402010201.

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