GUDIDData
eudamed_udi Primary ID: 05060120959003

Refill for EverFlo (UDI 05060120959003)

Manufactured by GVS Filter Technology UK Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Refill for EverFlo - Primary ID 05060120959003

Device Regulatory Overview

The Refill for EverFlo (Model/Catalog Number: 4100/735BAUB003/0001) is a medical device manufactured by GVS Filter Technology UK Limited. This product is indexed under FDA Product Code / Category Classification R040199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
4100/735BAUB003/0001
Product Code / EMDN
R040199
Device Name
Gas and Suction Filters
Database Sync Date
2026-08-09 16:28:48

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 Refill for EverFlo?

The registered manufacturer of record for Refill for EverFlo is GVS Filter Technology UK Limited.

What is the Primary UDI-DI identifier for Refill for EverFlo?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060120959003.

What classification code is assigned to this device?

This device is registered under product classification code R040199.

Programmatic Export

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

JSON API Endpoint