eudamed_udi
Primary ID: +M670107751900K
Unspecified Brand (UDI +M670107751900K)
Manufactured by Synergy Spine Solutions Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID +M670107751900K
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1077-5190) is a medical device manufactured by Synergy Spine Solutions Inc.. This product is indexed under FDA Product Code / Category Classification L091101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1077-5190
- Product Code / EMDN
- L091101
- Device Name
- Synergy Disc Remover
- Database Sync Date
- 2026-08-09 16:45:42
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Synergy Spine Solutions Inc..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +M670107751900K.
What classification code is assigned to this device?
This device is registered under product classification code L091101.
Similar Classification Devices (L091101)
Other Devices by Synergy Spine Solutions Inc.
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