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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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KIROFIX AND ACCESSORIES — 6 UDI-DI variants, MDR (Askorn Medical)

MD Atlas
Askorn Medical

Data from EUDAMED, last updated May 19, 2026

KIROFIX AND ACCESSORIES

3700751502266E

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Askorn Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3700751502266E
Device name: KIROFIX AND ACCESSORIES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Askorn Medical
SRN: FR-MF-000001716
Country: France
Email: contact@askorn.bzh
Phone: +33 2 23 35 53 35

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KR1B657MEV23RSC8M7ZB9NZP

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

Kirofix Ballast03700751500350
Kirofix Large03700751500329
Kirofix Medium03700751500343
Kirofix Ring03700751500367
Kirofix Small03700751500336
Kirofix Wrist03700751500374