eudamed_udi
Primary ID: 04260436070039
ELEC(R) (UDI 04260436070039)
Manufactured by HiPer Medical AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELEC(R) - Primary ID 04260436070039
Device Regulatory Overview
The ELEC(R) (Model/Catalog Number: 110030) is a medical device manufactured by HiPer Medical AG. This product is indexed under FDA Product Code / Category Classification P090804050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 110030
- Product Code / EMDN
- P090804050201
- Device Name
- femoral head
- Database Sync Date
- 2026-08-09 19:07:05
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 ELEC(R)?
The registered manufacturer of record for ELEC(R) is HiPer Medical AG.
What is the Primary UDI-DI identifier for ELEC(R)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260436070039.
What classification code is assigned to this device?
This device is registered under product classification code P090804050201.
Similar Classification Devices (P090804050201)
Other Devices by HiPer Medical AG
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