eudamed_udi Primary ID: 05903940702759

UPPER LIMB REHABILITATION DEVICE 881 (UDI 05903940702759)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The UPPER LIMB REHABILITATION DEVICE 881 (Model/Catalog Number: RF-881) is a medical device manufactured by REHA FUND Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification Y0580 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RF-881
Product Code / EMDN: Y0580
Device Name: PRZYRZĄD DO REHABILITACJI KOŃCZYN GÓRNYCH 881
Database Sync Date: 2026-08-09 17:15:08

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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Frequently Asked Questions

Who is the primary manufacturer of UPPER LIMB REHABILITATION DEVICE 881?

The registered manufacturer of record for UPPER LIMB REHABILITATION DEVICE 881 is REHA FUND Sp. z o.o..

What is the Primary UDI-DI identifier for UPPER LIMB REHABILITATION DEVICE 881?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903940702759.

What classification code is assigned to this device?

This device is registered under product classification code Y0580.

Similar Classification Devices (Y0580)

Other Devices by REHA FUND Sp. z o.o.

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