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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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Kinescan/IBV — 1 UDI-DI variant, MDR

MD Atlas
ASOCIACIÓN INSTITUTO DE BIOMECÁNICA DE VALENCIA (I.B.V.)

Data from EUDAMED, last updated May 31, 2026

Kinescan/IBV

8437020286Kinescan_PSFS

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: ASOCIACIÓN INSTITUTO DE BIOMECÁNICA DE VALENCIA (I.B.V.)

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8437020286Kinescan_PSFS
Device name: Kinescan/IBV
Device model: Kinescan_PS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: ASOCIACIÓN INSTITUTO DE BIOMECÁNICA DE VALENCIA (I.B.V.)
SRN: ES-MF-000004011
Country: Spain
Email: eudamed@ibv.org
Phone: +34 96 111 11 70

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KPTQ80S4FJ1NN9BDHYEGWNFE

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

Kinescan/IBV08437020286145