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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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Lancing device — 2 UDI-DI variants, MDR (DIAGNOSIS S.A.)

MD Atlas
DIAGNOSIS S.A.

Data from EUDAMED, last updated May 30, 2026

Lancing device

590758125lancetdeviceAZ

2 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: DIAGNOSIS S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590758125lancetdeviceAZ
Device name: Lancing device
Device model: Optilet PRO, Optilet MINI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: DIAGNOSIS S.A.
SRN: PL-MF-000014187
Country: Poland
Email: achomczuk@diagnosis.pl
Phone: +48 85 732 22 34

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H4MX9DTS4GD7CWEVT93R1RDS

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

Optilet Mini lancing device05907581254028
Optilet PRO lancing device05907581259306