gudid
Primary ID: SBM-1109-43
T-Handle AO-coupling (UDI SBM-1109-43)
Manufactured by Spierings Orthopaedics B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for T-Handle AO-coupling - Primary ID SBM-1109-43
Device Regulatory Overview
The T-Handle AO-coupling (Model/Catalog Number: SBM-1109-43) 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-1109-43
- 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 T-Handle AO-coupling?
The registered manufacturer of record for T-Handle AO-coupling is Spierings Orthopaedics B.V..
What is the Primary UDI-DI identifier for T-Handle AO-coupling?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBM-1109-43.
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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