eudamed_udi
Primary ID: 04260585132237
Elastus HydroZink (UDI 04260585132237)
Manufactured by Alegro Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elastus HydroZink - Primary ID 04260585132237
Device Regulatory Overview
The Elastus HydroZink (Model/Catalog Number: 71023 / 60023) is a medical device manufactured by Alegro Medical GmbH. This product is indexed under FDA Product Code / Category Classification M03020299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 71023 / 60023
- Product Code / EMDN
- M03020299
- Device Name
- ALEGRO Alginate
- Database Sync Date
- 2026-08-09 16:29:23
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 Elastus HydroZink?
The registered manufacturer of record for Elastus HydroZink is Alegro Medical GmbH.
What is the Primary UDI-DI identifier for Elastus HydroZink?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260585132237.
What classification code is assigned to this device?
This device is registered under product classification code M03020299.
Similar Classification Devices (M03020299)
Other Devices by Alegro Medical GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint