eudamed_udi
Primary ID: 08055728030121
ELEKTRA (UDI 08055728030121)
Manufactured by Dedalus Italia SpA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELEKTRA - Primary ID 08055728030121
Device Regulatory Overview
The ELEKTRA (Model/Catalog Number: ELEKTRA) is a medical device manufactured by Dedalus Italia SpA. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ELEKTRA
- Product Code / EMDN
- V92
- Device Name
- ELEKTRA
- Database Sync Date
- 2026-08-09 16:29:54
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 ELEKTRA?
The registered manufacturer of record for ELEKTRA is Dedalus Italia SpA.
What is the Primary UDI-DI identifier for ELEKTRA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055728030121.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
Other Devices by Dedalus Italia SpA
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