GUDIDData
eudamed_udi Primary ID: 06945764440270

Multi-Patient Syringe System (UDI 06945764440270)

Manufactured by Shenzhen Antmed Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Multi-Patient Syringe System - Primary ID 06945764440270

Device Regulatory Overview

The Multi-Patient Syringe System (Model/Catalog Number: R400307) is a medical device manufactured by Shenzhen Antmed Co., Ltd. This product is indexed under FDA Product Code / Category Classification A020102010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
R400307
Product Code / EMDN
A020102010102
Device Name
Multi-Patient Syringe System
Database Sync Date
2026-08-09 16:28:47

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Multi-Patient Syringe System?

The registered manufacturer of record for Multi-Patient Syringe System is Shenzhen Antmed Co., Ltd.

What is the Primary UDI-DI identifier for Multi-Patient Syringe System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945764440270.

What classification code is assigned to this device?

This device is registered under product classification code A020102010102.

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