GUDIDData
eudamed_udi Primary ID: 07290109155357

Infuzní pumpa Sapphire (UDI 07290109155357)

Manufactured by Eitan Medical Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Infuzní pumpa Sapphire - Primary ID 07290109155357

Device Regulatory Overview

The Infuzní pumpa Sapphire (Model/Catalog Number: 15031-000-0017) is a medical device manufactured by Eitan Medical Ltd. This product is indexed under FDA Product Code / Category Classification Z12030301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
15031-000-0017
Product Code / EMDN
Z12030301
Device Name
Sapphire Infusion Pump
Database Sync Date
2026-08-09 16:28:54

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 Infuzní pumpa Sapphire?

The registered manufacturer of record for Infuzní pumpa Sapphire is Eitan Medical Ltd.

What is the Primary UDI-DI identifier for Infuzní pumpa Sapphire?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07290109155357.

What classification code is assigned to this device?

This device is registered under product classification code Z12030301.

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