Oxygen demand valve kit with regulator (UDI 05052270000193)
Manufactured by B.N.O.S. Meditech Limited
Device Regulatory Overview
The Oxygen demand valve kit with regulator (Model/Catalog Number: 910-3021-00) 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
- 910-3021-00
- Product Code / EMDN
- V0501
- Device Name
- Demand Valve
- Database Sync Date
- 2026-08-09 16:59:26
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Oxygen demand valve kit with regulator?
The registered manufacturer of record for Oxygen demand valve kit with regulator is B.N.O.S. Meditech Limited.
What is the Primary UDI-DI identifier for Oxygen demand valve kit with regulator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05052270000193.
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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