eudamed_udi
Primary ID: 03701459811717
SANGLE M2R/S (UDI 03701459811717)
Manufactured by GROUPE SOBER SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SANGLE M2R/S - Primary ID 03701459811717
Device Regulatory Overview
The SANGLE M2R/S (Model/Catalog Number: SANGLE M2R/S) is a medical device manufactured by GROUPE SOBER SAS. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SANGLE M2R/S
- Product Code / EMDN
- Y060380
- Device Name
- SANGLE M2R/S
- Database Sync Date
- 2026-08-09 16:44:50
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SANGLE M2R/S?
The registered manufacturer of record for SANGLE M2R/S is GROUPE SOBER SAS.
What is the Primary UDI-DI identifier for SANGLE M2R/S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701459811717.
What classification code is assigned to this device?
This device is registered under product classification code Y060380.
Similar Classification Devices (Y060380)
Other Devices by GROUPE SOBER SAS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint