eudamed_udi
Primary ID: 08052532833108
FIXA LARUS (UDI 08052532833108)
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 FIXA LARUS - Primary ID 08052532833108
Device Regulatory Overview
The FIXA LARUS (Model/Catalog Number: 0746568) is a medical device manufactured by Adler Ortho S.p.A. This product is indexed under FDA Product Code / Category Classification P090803010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0746568
- Product Code / EMDN
- P090803010201
- Device Name
- FIXA LARUS PRESS-FIT CUP Ti+HA COATED SIZE 68 GR D
- Database Sync Date
- 2026-08-09 16:29:50
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 FIXA LARUS?
The registered manufacturer of record for FIXA LARUS is Adler Ortho S.p.A.
What is the Primary UDI-DI identifier for FIXA LARUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052532833108.
What classification code is assigned to this device?
This device is registered under product classification code P090803010201.
Similar Classification Devices (P090803010201)
Other Devices by Adler Ortho S.p.A
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