eudamed_udi
Primary ID: 03701675300606
Cadre Auvert nu 310 x 400mm (UDI 03701675300606)
Manufactured by Ets Claude LASSERTEUX S.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cadre Auvert nu 310 x 400mm - Primary ID 03701675300606
Device Regulatory Overview
The Cadre Auvert nu 310 x 400mm (Model/Catalog Number: 901800.01) is a medical device manufactured by Ets Claude LASSERTEUX S.A. This product is indexed under FDA Product Code / Category Classification L0318 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 901800.01
- Product Code / EMDN
- L0318
- Device Name
- Cadre Auvert nu 310 x 400mm
- Database Sync Date
- 2026-08-09 16:49:45
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 Cadre Auvert nu 310 x 400mm?
The registered manufacturer of record for Cadre Auvert nu 310 x 400mm is Ets Claude LASSERTEUX S.A.
What is the Primary UDI-DI identifier for Cadre Auvert nu 310 x 400mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701675300606.
What classification code is assigned to this device?
This device is registered under product classification code L0318.
Similar Classification Devices (L0318)
Other Devices by Ets Claude LASSERTEUX S.A
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint