GUDIDData
eudamed_udi Primary ID: 04710810114731

Filter, Hydrophobic 4F, 4M (UDI 04710810114731)

Manufactured by GaleMed Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Filter, Hydrophobic 4F, 4M - Primary ID 04710810114731

Device Regulatory Overview

The Filter, Hydrophobic 4F, 4M (Model/Catalog Number: AF0013) is a medical device manufactured by GaleMed Corporation. This product is indexed under FDA Product Code / Category Classification R03010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AF0013
Product Code / EMDN
R03010201
Device Name
Connector
Database Sync Date
2026-08-09 16:29:09

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 Filter, Hydrophobic 4F, 4M?

The registered manufacturer of record for Filter, Hydrophobic 4F, 4M is GaleMed Corporation.

What is the Primary UDI-DI identifier for Filter, Hydrophobic 4F, 4M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710810114731.

What classification code is assigned to this device?

This device is registered under product classification code R03010201.

Programmatic Export

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

JSON API Endpoint