gudid
Primary ID: SBM-0503-18
Inverted Reamer-AO 42 (UDI SBM-0503-18)
Manufactured by Spierings Orthopaedics B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inverted Reamer-AO 42 - Primary ID SBM-0503-18
Device Regulatory Overview
The Inverted Reamer-AO 42 (Model/Catalog Number: SBM-0503-18) is a medical device manufactured by Spierings Orthopaedics B.V.. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SBM-0503-18
- Product Code / EMDN
- LXH
- Device Name
- Database Sync Date
- 2026-08-09 09:26:43
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 Inverted Reamer-AO 42?
The registered manufacturer of record for Inverted Reamer-AO 42 is Spierings Orthopaedics B.V..
What is the Primary UDI-DI identifier for Inverted Reamer-AO 42?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBM-0503-18.
What classification code is assigned to this device?
This device is registered under product classification code LXH.
Similar Classification Devices (LXH)
Other Devices by Spierings Orthopaedics B.V.
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