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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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OAK — 1 UDI-DI variant, MDR (Khymeia S.r.l.)

MD Atlas
Khymeia S.r.l.

Data from EUDAMED, last updated May 31, 2026

OAK

805071490OAKHC

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: Khymeia S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805071490OAKHC
Device name: OAK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Khymeia S.r.l.
SRN: IT-MF-000035617
Country: Italy
Email: f.piron@khymeia.com
Phone: 0498935107

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KAZPNFPQEKY2JXX224V7Y90Y

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

OAK08050714900143