gudid
Primary ID: SPORT
HYBRIBOARD (UDI SPORT)
Manufactured by FLAMOR SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HYBRIBOARD - Primary ID SPORT
Device Regulatory Overview
The HYBRIBOARD (Model/Catalog Number: SPORT) is a medical device manufactured by FLAMOR SRL. This product is indexed under FDA Product Code / Category Classification FPP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPORT
- Product Code / EMDN
- FPP
- Device Name
- The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as is the case with basket stretchers, by the vertical walls of the stretcher being 20-25cm high.
- Database Sync Date
- 2026-08-09 09:04:28
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 HYBRIBOARD?
The registered manufacturer of record for HYBRIBOARD is FLAMOR SRL.
What is the Primary UDI-DI identifier for HYBRIBOARD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SPORT.
What classification code is assigned to this device?
This device is registered under product classification code FPP.
Similar Classification Devices (FPP)
Other Devices by FLAMOR SRL
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