GUDIDData
eudamed_udi Primary ID: 50052270000018

MicroVENT Industrial resuscitation kit with soft case. (UDI 50052270000018)

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

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MicroVENT Industrial resuscitation kit with soft case. - Primary ID 50052270000018

Device Regulatory Overview

The MicroVENT Industrial resuscitation kit with soft case. (Model/Catalog Number: 670-0309-01) 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
670-0309-01
Product Code / EMDN
V0501
Device Name
MicroVENT
Database Sync Date
2026-08-09 18:20:30

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 MicroVENT Industrial resuscitation kit with soft case.?

The registered manufacturer of record for MicroVENT Industrial resuscitation kit with soft case. is B.N.O.S. Meditech Limited.

What is the Primary UDI-DI identifier for MicroVENT Industrial resuscitation kit with soft case.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50052270000018.

What classification code is assigned to this device?

This device is registered under product classification code V0501.

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