gudid
Primary ID: NAV-IN 51 24-N
PERLA NAV (UDI NAV-IN 51 24-N)
Manufactured by SpineArt SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PERLA NAV - Primary ID NAV-IN 51 24-N
Device Regulatory Overview
The PERLA NAV (Model/Catalog Number: NAV-IN 51 24-N) is a medical device manufactured by SpineArt SA. This product is indexed under FDA Product Code / Category Classification OLO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NAV-IN 51 24-N
- Product Code / EMDN
- OLO
- Device Name
- DRILL 2.4
- Database Sync Date
- 2026-08-09 09:07:25
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 PERLA NAV?
The registered manufacturer of record for PERLA NAV is SpineArt SA.
What is the Primary UDI-DI identifier for PERLA NAV?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NAV-IN 51 24-N.
What classification code is assigned to this device?
This device is registered under product classification code OLO.
Similar Classification Devices (OLO)
Other Devices by SpineArt SA
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