GUDIDData
gudid Primary ID: DOAY-2135

Healgen (UDI DOAY-2135)

Manufactured by Healgen Scientific Limited Liability Company

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Healgen - Primary ID DOAY-2135

Device Regulatory Overview

The Healgen (Model/Catalog Number: DOAY-2135) is a medical device manufactured by Healgen Scientific Limited Liability Company. This product is indexed under FDA Product Code / Category Classification LCM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DOAY-2135
Product Code / EMDN
LCM
Device Name
13 Panel DOA Test Dipcard
Database Sync Date
2026-08-09 09:31:32

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 Healgen?

The registered manufacturer of record for Healgen is Healgen Scientific Limited Liability Company.

What is the Primary UDI-DI identifier for Healgen?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DOAY-2135.

What classification code is assigned to this device?

This device is registered under product classification code LCM.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint