eudamed_udi
Primary ID: 04260661458596
I6110017 (UDI 04260661458596)
Manufactured by provita medical gmbh & co. kg
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for I6110017 - Primary ID 04260661458596
Device Regulatory Overview
The I6110017 (Model/Catalog Number: 177904) is a medical device manufactured by provita medical gmbh & co. kg. This product is indexed under FDA Product Code / Category Classification Z12030380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 177904
- Product Code / EMDN
- Z12030380
- Device Name
- IV-stand mobile + accessories
- Database Sync Date
- 2026-08-09 16:29:02
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 I6110017?
The registered manufacturer of record for I6110017 is provita medical gmbh & co. kg.
What is the Primary UDI-DI identifier for I6110017?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260661458596.
What classification code is assigned to this device?
This device is registered under product classification code Z12030380.
Similar Classification Devices (Z12030380)
Other Devices by provita medical gmbh & co. kg
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint