eudamed_udi
Primary ID: 07640187463378
SALTI Anterolateral Template (UDI 07640187463378)
Manufactured by Bonebridge AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SALTI Anterolateral Template - Primary ID 07640187463378
Device Regulatory Overview
The SALTI Anterolateral Template (Model/Catalog Number: B-420042) is a medical device manufactured by Bonebridge AG. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B-420042
- Product Code / EMDN
- L091001
- Device Name
- Bonebridge Instrument-IIa
- Database Sync Date
- 2026-08-09 16:29:01
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 SALTI Anterolateral Template?
The registered manufacturer of record for SALTI Anterolateral Template is Bonebridge AG.
What is the Primary UDI-DI identifier for SALTI Anterolateral Template?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640187463378.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
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