GUDIDData
eudamed_udi Primary ID: 06430053264182

UCAST (UDI 06430053264182)

Manufactured by Dassiet Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UCAST - Primary ID 06430053264182

Device Regulatory Overview

The UCAST (Model/Catalog Number: A-KNEE) is a medical device manufactured by Dassiet Oy. This product is indexed under FDA Product Code / Category Classification M03050201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A-KNEE
Product Code / EMDN
M03050201
Device Name
UCAST orthosis
Database Sync Date
2026-08-09 16:49:34

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of UCAST?

The registered manufacturer of record for UCAST is Dassiet Oy.

What is the Primary UDI-DI identifier for UCAST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430053264182.

What classification code is assigned to this device?

This device is registered under product classification code M03050201.

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