GUDIDData
eudamed_udi Primary ID: 06954414798043

MAGICL T3 (CLIA) (UDI 06954414798043)

Manufactured by Getein Biotech, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAGICL T3 (CLIA) - Primary ID 06954414798043

Device Regulatory Overview

The MAGICL T3 (CLIA) (Model/Catalog Number: /) is a medical device manufactured by Getein Biotech, Inc.. This product is indexed under FDA Product Code / Category Classification W01020405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
/
Product Code / EMDN
W01020405
Device Name
MAGICL T3 (CLIA)
Database Sync Date
2026-08-09 16:59:49

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 MAGICL T3 (CLIA)?

The registered manufacturer of record for MAGICL T3 (CLIA) is Getein Biotech, Inc..

What is the Primary UDI-DI identifier for MAGICL T3 (CLIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414798043.

What classification code is assigned to this device?

This device is registered under product classification code W01020405.

Programmatic Export

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

JSON API Endpoint