GUDIDData
eudamed_udi Primary ID: 06923980102110

HMEF w/Luer, 22F/15M, 22/15mm (UDI 06923980102110)

Manufactured by GaleMed (Xiamen) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HMEF w/Luer, 22F/15M, 22/15mm - Primary ID 06923980102110

Device Regulatory Overview

The HMEF w/Luer, 22F/15M, 22/15mm (Model/Catalog Number: AH0041) is a medical device manufactured by GaleMed (Xiamen) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R040101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AH0041
Product Code / EMDN
R040101
Device Name
Disposable Filter
Database Sync Date
2026-08-09 16:48:44

Full Regulatory Attributes

πŸ”’ 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 HMEF w/Luer, 22F/15M, 22/15mm?

The registered manufacturer of record for HMEF w/Luer, 22F/15M, 22/15mm is GaleMed (Xiamen) Co., Ltd..

What is the Primary UDI-DI identifier for HMEF w/Luer, 22F/15M, 22/15mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06923980102110.

What classification code is assigned to this device?

This device is registered under product classification code R040101.

Programmatic Export

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

JSON API Endpoint