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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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AVIOR Anke and knee joint… — 1 UDI-DI variant, MDR (Terma Sp. z o.o.)

MD Atlas
Terma Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

AVIOR Anke and knee joint rehabilitation device

5903918WDAVI-0001U9

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Terma Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5903918WDAVI-0001U9
Device name: AVIOR Anke and knee joint rehabilitation device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: Terma Sp. z o.o.
SRN: PL-MF-000021635
Country: Poland
Email: izabela.adamska@termagroup.pl
Phone: 607451605

Variants by status

UDI-DI variants

1 UDI-DI variant

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Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

AVIOR Ankle and knee rehabilitation device05901804055829