eudamed_udi
Primary ID: 10705034194172
MOSS MIAMI SPINE SYSTEM (UDI 10705034194172)
Manufactured by Medos International SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MOSS MIAMI SPINE SYSTEM - Primary ID 10705034194172
Device Regulatory Overview
The MOSS MIAMI SPINE SYSTEM (Model/Catalog Number: 275015100) is a medical device manufactured by Medos International SARL. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 275015100
- Product Code / EMDN
- L091001
- Device Name
- Moss Miami Alignment Guide Driver Ring Tab Key Head Positioner Rod Pusher Screwdriver Nut Tightener
- Database Sync Date
- 2026-08-09 16:28:54
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 MOSS MIAMI SPINE SYSTEM?
The registered manufacturer of record for MOSS MIAMI SPINE SYSTEM is Medos International SARL.
What is the Primary UDI-DI identifier for MOSS MIAMI SPINE SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705034194172.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
Other Devices by Medos International SARL
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