eudamed_udi
Primary ID: 85942023204144
DOMEO M (UDI 85942023204144)
Manufactured by PROMA REHA, s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DOMEO M - Primary ID 85942023204144
Device Regulatory Overview
The DOMEO M (Model/Catalog Number: DOMEO-M-85) is a medical device manufactured by PROMA REHA, s.r.o.. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DOMEO-M-85
- Product Code / EMDN
- V080602
- Device Name
- Kinetic bed
- Database Sync Date
- 2026-08-09 16:29:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DOMEO M?
The registered manufacturer of record for DOMEO M is PROMA REHA, s.r.o..
What is the Primary UDI-DI identifier for DOMEO M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 85942023204144.
What classification code is assigned to this device?
This device is registered under product classification code V080602.
Similar Classification Devices (V080602)
Other Devices by PROMA REHA, s.r.o.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint