gudid
Primary ID: 17-135125-09
ARx SAI (UDI 17-135125-09)
Manufactured by Life Spine, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARx SAI - Primary ID 17-135125-09
Device Regulatory Overview
The ARx SAI (Model/Catalog Number: 17-135125-09) is a medical device manufactured by Life Spine, Inc.. This product is indexed under FDA Product Code / Category Classification OUR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 17-135125-09
- Product Code / EMDN
- OUR
- Device Name
- Database Sync Date
- 2026-08-09 09:02:28
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 ARx SAI?
The registered manufacturer of record for ARx SAI is Life Spine, Inc..
What is the Primary UDI-DI identifier for ARx SAI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 17-135125-09.
What classification code is assigned to this device?
This device is registered under product classification code OUR.
Similar Classification Devices (OUR)
Other Devices by Life Spine, Inc.
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