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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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Intuy Knee — 5 UDI-DI variants, MDR (Reboocon Bionics B.V.)

MD Atlas
Reboocon Bionics B.V.

Data from EUDAMED, last updated May 30, 2026

Intuy Knee

87202994598ILK98

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Reboocon Bionics B.V.

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 87202994598ILK98
Device name: Intuy Knee
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: Reboocon Bionics B.V.
SRN: NL-MF-000000239
Country: Netherlands
Email: info@rbionics.com
Phone: +31636275861

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FYVTR9D52ZQ66539GXS3FWZ8

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

ILK-1B08720299459809
ILK-1W08720299459816
IK1N08720299459830
IK1P08720299459823
1K1R08720299459847