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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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AKUTOL™ spray — 4 UDI-DI variants, MDR (AVEFLOR, a.s.)

MD Atlas
AVEFLOR, a.s.

Data from EUDAMED, last updated May 23, 2026

AKUTOL™ spray

859401370Z08NJ

4 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: AVEFLOR, a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859401370Z08NJ
Device name: AKUTOL™ spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: AVEFLOR, a.s.
SRN: CZ-MF-000003103
Country: Czechia
Email: aveflor@aveflor.cz
Phone: +420 493 551 111

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7RHE8SPKQCJKPN9YDRR6DSM

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

Z29000608594013703819
Z29000008594013703352
Z08000808594013701952
Z080050 08594013705110