eudamed_udi
Primary ID: 06429810980021
DBC LTR Lumbar Thoracic Rotation (UDI 06429810980021)
Manufactured by DBC Global Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DBC LTR Lumbar Thoracic Rotation - Primary ID 06429810980021
Device Regulatory Overview
The DBC LTR Lumbar Thoracic Rotation (Model/Catalog Number: LTR6120) is a medical device manufactured by DBC Global Oy. This product is indexed under FDA Product Code / Category Classification Z120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LTR6120
- Product Code / EMDN
- Z120602
- Device Name
- DBC LTR Lumbar Thoracic Rotation
- Database Sync Date
- 2026-08-09 16:29:07
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 DBC LTR Lumbar Thoracic Rotation?
The registered manufacturer of record for DBC LTR Lumbar Thoracic Rotation is DBC Global Oy.
What is the Primary UDI-DI identifier for DBC LTR Lumbar Thoracic Rotation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06429810980021.
What classification code is assigned to this device?
This device is registered under product classification code Z120602.
Similar Classification Devices (Z120602)
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