eudamed_udi Primary ID: 05052270000100

Entonox demand valve kit without regulator (UDI 05052270000100)

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 Entonox demand valve kit without regulator (Model/Catalog Number: 900-1021-00) 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: 900-1021-00
Product Code / EMDN: V0501
Device Name: Demand Valve
Database Sync Date: 2026-08-09 17:12:40

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 Entonox demand valve kit without regulator?

The registered manufacturer of record for Entonox demand valve kit without regulator is B.N.O.S. Meditech Limited.

What is the Primary UDI-DI identifier for Entonox demand valve kit without regulator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05052270000100.

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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