GUDIDData
eudamed_udi Primary ID: 06958627548211

VENTURI MASK (UDI 06958627548211)

Manufactured by Ningbo Greetmed Medical Instruments Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VENTURI MASK - Primary ID 06958627548211

Device Regulatory Overview

The VENTURI MASK (Model/Catalog Number: GT010-150-3) is a medical device manufactured by Ningbo Greetmed Medical Instruments Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification R03010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GT010-150-3
Product Code / EMDN
R03010201
Device Name
OXYGEN MASK
Database Sync Date
2026-08-09 16:29:19

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 VENTURI MASK?

The registered manufacturer of record for VENTURI MASK is Ningbo Greetmed Medical Instruments Co.,Ltd..

What is the Primary UDI-DI identifier for VENTURI MASK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958627548211.

What classification code is assigned to this device?

This device is registered under product classification code R03010201.

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