gudid
Primary ID: 11732234122
Elecsys LH (UDI 11732234122)
Manufactured by Roche Diagnostics GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elecsys LH - Primary ID 11732234122
Device Regulatory Overview
The Elecsys LH (Model/Catalog Number: 11732234122) is a medical device manufactured by Roche Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification CEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11732234122
- Product Code / EMDN
- CEP
- Device Name
- Database Sync Date
- 2026-08-09 09:33:50
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 Elecsys LH?
The registered manufacturer of record for Elecsys LH is Roche Diagnostics GmbH.
What is the Primary UDI-DI identifier for Elecsys LH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11732234122.
What classification code is assigned to this device?
This device is registered under product classification code CEP.
Similar Classification Devices (CEP)
Other Devices by Roche Diagnostics GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint