eudamed_udi Primary ID: 05052270000025

MicroVENT Utility resuscitation kit. (UDI 05052270000025)

Manufactured by B.N.O.S. Meditech Limited

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MicroVENT Utility resuscitation kit. (Model/Catalog Number: 670-0340-01) is a medical device manufactured by B.N.O.S. Meditech Limited. This product is indexed under FDA Product Code / Category Classification V0501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 670-0340-01
Product Code / EMDN: V0501
Device Name: MicroVENT
Database Sync Date: 2026-08-09 18:59:38

Full Regulatory Attributes

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{
    "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 MicroVENT Utility resuscitation kit.?

The registered manufacturer of record for MicroVENT Utility resuscitation kit. is B.N.O.S. Meditech Limited.

What is the Primary UDI-DI identifier for MicroVENT Utility resuscitation kit.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05052270000025.

What classification code is assigned to this device?

This device is registered under product classification code V0501.

Similar Classification Devices (V0501)

Other Devices by B.N.O.S. Meditech Limited

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