GUDIDData
eudamed_udi Primary ID: 07333066015545

EliA Ro60 Well (UDI 07333066015545)

Manufactured by Phadia AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EliA Ro60 Well - Primary ID 07333066015545

Device Regulatory Overview

The EliA Ro60 Well (Model/Catalog Number: 14-5525-01) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification W0102100112 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
14-5525-01
Product Code / EMDN
W0102100112
Device Name
EliA Ro60
Database Sync Date
2026-08-09 17:26:24

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 EliA Ro60 Well?

The registered manufacturer of record for EliA Ro60 Well is Phadia AB.

What is the Primary UDI-DI identifier for EliA Ro60 Well?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07333066015545.

What classification code is assigned to this device?

This device is registered under product classification code W0102100112.

Programmatic Export

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

JSON API Endpoint