GUDIDData
eudamed_udi Primary ID: 05051223037552

Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector (UDI 05051223037552)

Manufactured by SHANDONG ZHENFU MEDICAL DEVICE CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector - Primary ID 05051223037552

Device Regulatory Overview

The Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector (Model/Catalog Number: PS3602A) is a medical device manufactured by SHANDONG ZHENFU MEDICAL DEVICE CO., LTD.. This product is indexed under FDA Product Code / Category Classification K0180 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PS3602A
Product Code / EMDN
K0180
Device Name
Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector
Database Sync Date
2026-08-09 16:51:36

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 Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector?

The registered manufacturer of record for Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector is SHANDONG ZHENFU MEDICAL DEVICE CO., LTD..

What is the Primary UDI-DI identifier for Essential Insufflation Filter/Tubing Set with Push Fit Funnel Connector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051223037552.

What classification code is assigned to this device?

This device is registered under product classification code K0180.

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