eudamed_udi
Primary ID: 06944413836112
Lyse (UDI 06944413836112)
Manufactured by Edan Instruments,Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lyse - Primary ID 06944413836112
Device Regulatory Overview
The Lyse (Model/Catalog Number: HL91D) is a medical device manufactured by Edan Instruments,Inc.. This product is indexed under FDA Product Code / Category Classification W0103010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HL91D
- Product Code / EMDN
- W0103010105
- Device Name
- Lyse
- Database Sync Date
- 2026-08-09 16:28:53
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 Lyse?
The registered manufacturer of record for Lyse is Edan Instruments,Inc..
What is the Primary UDI-DI identifier for Lyse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944413836112.
What classification code is assigned to this device?
This device is registered under product classification code W0103010105.
Similar Classification Devices (W0103010105)
Other Devices by Edan Instruments,Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint