GUDIDData
eudamed_udi Primary ID: 00841517106515

C5-1 (UDI 00841517106515)

Manufactured by Fujifilm Sonosite, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C5-1 - Primary ID 00841517106515

Device Regulatory Overview

The C5-1 (Model/Catalog Number: P23119-20A) is a medical device manufactured by Fujifilm Sonosite, Inc.. This product is indexed under FDA Product Code / Category Classification Z110402010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
P23119-20A
Product Code / EMDN
Z110402010201
Device Name
TRANSDUCER, C5-1
Database Sync Date
2026-08-09 16:51:52

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of C5-1?

The registered manufacturer of record for C5-1 is Fujifilm Sonosite, Inc..

What is the Primary UDI-DI identifier for C5-1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841517106515.

What classification code is assigned to this device?

This device is registered under product classification code Z110402010201.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint