GUDIDData
eudamed_udi Primary ID: 04751011630446

SanaSet (UDI 04751011630446)

Manufactured by SIA FARMEKO

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SanaSet - Primary ID 04751011630446

Device Regulatory Overview

The SanaSet (Model/Catalog Number: 630446) is a medical device manufactured by SIA FARMEKO. This product is indexed under FDA Product Code / Category Classification T04010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
630446
Product Code / EMDN
T04010201
Device Name
SanaSet
Database Sync Date
2026-08-09 17:23:12

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 SanaSet?

The registered manufacturer of record for SanaSet is SIA FARMEKO.

What is the Primary UDI-DI identifier for SanaSet?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04751011630446.

What classification code is assigned to this device?

This device is registered under product classification code T04010201.

Programmatic Export

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

JSON API Endpoint