eudamed_udi
Primary ID: 08052532833849
OMNIA (UDI 08052532833849)
Manufactured by Adler Ortho S.p.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OMNIA - Primary ID 08052532833849
Device Regulatory Overview
The OMNIA (Model/Catalog Number: 0760008) is a medical device manufactured by Adler Ortho S.p.A. This product is indexed under FDA Product Code / Category Classification P09088007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0760008
- Product Code / EMDN
- P09088007
- Device Name
- PLUG FOR OMNIA ILIAC STEM SCREW
- Database Sync Date
- 2026-08-09 16:51:29
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 OMNIA?
The registered manufacturer of record for OMNIA is Adler Ortho S.p.A.
What is the Primary UDI-DI identifier for OMNIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052532833849.
What classification code is assigned to this device?
This device is registered under product classification code P09088007.
Similar Classification Devices (P09088007)
Other Devices by Adler Ortho S.p.A
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