eudamed_udi
Primary ID: 10705034556253
CONDUIT Lateral (UDI 10705034556253)
Manufactured by Medos International SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONDUIT Lateral - Primary ID 10705034556253
Device Regulatory Overview
The CONDUIT Lateral (Model/Catalog Number: LET01061T) 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
- LET01061T
- Product Code / EMDN
- L091001
- Device Name
- Conduit Trial
- Database Sync Date
- 2026-08-09 16:28:58
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 CONDUIT Lateral?
The registered manufacturer of record for CONDUIT Lateral is Medos International SARL.
What is the Primary UDI-DI identifier for CONDUIT Lateral?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705034556253.
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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