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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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Sensorki TULLO — 6 UDI-DI variants, MDR (TULLO KATARZYNA ABRAMCZUK)

MD Atlas
TULLO KATARZYNA ABRAMCZUK

Data from EUDAMED, last updated May 30, 2026

Sensorki TULLO

590509477sensorkiM8

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: TULLO KATARZYNA ABRAMCZUK

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590509477sensorkiM8
Device name: Sensorki TULLO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: TULLO KATARZYNA ABRAMCZUK
SRN: PL-MF-000051080
Country: Poland
Email: biuro@tullo.pl
Phone: +48 600 363 105

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KGZAPP29CADAFVZ48REETNB3

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

80405905094778048
80005905094778000
80305905094778031
80205905094778024
80105905094778017
80505905094778055