NEXUS - MATERASSO DEPRESSIONE ANTIRETRAZIONE (UDI 08057711231546)
Manufactured by Spencer Italia s.r.l.
Device Regulatory Overview
The NEXUS - MATERASSO DEPRESSIONE ANTIRETRAZIONE (Model/Catalog Number: QM22900) is a medical device manufactured by Spencer Italia s.r.l.. This product is indexed under FDA Product Code / Category Classification V0804 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QM22900
- Product Code / EMDN
- V0804
- Device Name
- Vacuum mattresses
- Database Sync Date
- 2026-08-09 16:30:21
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 NEXUS - MATERASSO DEPRESSIONE ANTIRETRAZIONE?
The registered manufacturer of record for NEXUS - MATERASSO DEPRESSIONE ANTIRETRAZIONE is Spencer Italia s.r.l..
What is the Primary UDI-DI identifier for NEXUS - MATERASSO DEPRESSIONE ANTIRETRAZIONE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057711231546.
What classification code is assigned to this device?
This device is registered under product classification code V0804.
Similar Classification Devices (V0804)
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