eudamed_udi
Primary ID: 04719872331087
Zimmer Group (UDI 04719872331087)
Manufactured by ZMI Electronics Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zimmer Group - Primary ID 04719872331087
Device Regulatory Overview
The Zimmer Group (Model/Catalog Number: LP1117-252-22F) is a medical device manufactured by ZMI Electronics Ltd.. This product is indexed under FDA Product Code / Category Classification Z12062880 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LP1117-252-22F
- Product Code / EMDN
- Z12062880
- Device Name
- Rubber Electrode
- Database Sync Date
- 2026-08-09 16:30:42
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 Zimmer Group?
The registered manufacturer of record for Zimmer Group is ZMI Electronics Ltd..
What is the Primary UDI-DI identifier for Zimmer Group?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719872331087.
What classification code is assigned to this device?
This device is registered under product classification code Z12062880.
Similar Classification Devices (Z12062880)
Other Devices by ZMI Electronics Ltd.
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