eudamed_udi
Primary ID: 04260123936365
I2072592 (UDI 04260123936365)
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 I2072592 - Primary ID 04260123936365
Device Regulatory Overview
The I2072592 (Model/Catalog Number: 176400) 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
- 176400
- Product Code / EMDN
- Z12030380
- Device Name
- Ceiling IV poles
- Database Sync Date
- 2026-08-09 16:45:46
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of I2072592?
The registered manufacturer of record for I2072592 is provita medical gmbh & co. kg.
What is the Primary UDI-DI identifier for I2072592?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260123936365.
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
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