eudamed_udi
Primary ID: 10705034532721
SYMPHONY OCT SYSTEM (UDI 10705034532721)
Manufactured by Medos International SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SYMPHONY OCT SYSTEM - Primary ID 10705034532721
Device Regulatory Overview
The SYMPHONY OCT SYSTEM (Model/Catalog Number: 2020-33-102) is a medical device manufactured by Medos International SARL. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2020-33-102
- Product Code / EMDN
- L0915
- Device Name
- ORTHOPAEDIC SURGERY DIALATORS AND RETRACTORS - SYMPHONY OCT INSTRUMENTS
- Database Sync Date
- 2026-08-09 16:29:29
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 SYMPHONY OCT SYSTEM?
The registered manufacturer of record for SYMPHONY OCT SYSTEM is Medos International SARL.
What is the Primary UDI-DI identifier for SYMPHONY OCT SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705034532721.
What classification code is assigned to this device?
This device is registered under product classification code L0915.
Similar Classification Devices (L0915)
Other Devices by Medos International SARL
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