eudamed_udi
Primary ID: 85942023201242
INVENT (UDI 85942023201242)
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 INVENT - Primary ID 85942023201242
Device Regulatory Overview
The INVENT (Model/Catalog Number: INVENT-2C) is a medical device manufactured by PROMA REHA, s.r.o.. This product is indexed under FDA Product Code / Category Classification V08060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INVENT-2C
- Product Code / EMDN
- V08060101
- Device Name
- Kinetic bed
- Database Sync Date
- 2026-08-09 16:46:59
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 INVENT?
The registered manufacturer of record for INVENT is PROMA REHA, s.r.o..
What is the Primary UDI-DI identifier for INVENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 85942023201242.
What classification code is assigned to this device?
This device is registered under product classification code V08060101.
Similar Classification Devices (V08060101)
Other Devices by PROMA REHA, s.r.o.
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