Provox Life Night HME Experience (UDI 8072)
Manufactured by Atos Medical AB
Device Regulatory Overview
The Provox Life Night HME Experience (Model/Catalog Number: 8072) is a medical device manufactured by Atos Medical AB. This product is indexed under FDA Product Code / Category Classification BYD within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients breathing through a trac...
Technical Specifications
- Model Number
- 8072
- Product Code / EMDN
- BYD
- Device Name
- Provox Life HMEs are single use heat and moisture exchangers for patients breathing through a tracheostoma
- Database Sync Date
- 2026-08-09 09:10:28
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 Provox Life Night HME Experience?
The registered manufacturer of record for Provox Life Night HME Experience is Atos Medical AB.
What is the Primary UDI-DI identifier for Provox Life Night HME Experience?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8072.
What classification code is assigned to this device?
This device is registered under product classification code BYD.
Similar Classification Devices (BYD)
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