Provox ShowerAid (UDI 7260)
Manufactured by Atos Medical AB
Device Regulatory Overview
The Provox ShowerAid (Model/Catalog Number: 7260) 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
- 7260
- Product Code / EMDN
- BYD
- Device Name
- Provox ShowerAid is used to temporarily replace the HME during showering. The ShowerAid can be placed in all Provox appliance holders.
- 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 ShowerAid?
The registered manufacturer of record for Provox ShowerAid is Atos Medical AB.
What is the Primary UDI-DI identifier for Provox ShowerAid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7260.
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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