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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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Lipotris™ — 5 UDI-DI variants, MDR

MD Atlas
"Biovico" Spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 31, 2026

Lipotris™

5902020847LPT6D

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: "Biovico" Spółka z ograniczoną odpowiedzialnością

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Device characteristics

Implantable

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 1434-MDR-040/2025
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: Dec 16, 2025 → Dec 15, 2030

Identity & classification

Basic UDI-DI: 5902020847LPT6D
Device name: Lipotris™
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Sep 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: "Biovico" Spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000010559
Country: Poland
Email: office@biovico.com
Phone: +48 58 660 44 88

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K62CMW1EA0WHHDS0V17N7TGC

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

PRO0081905907381850567
PRO0081905907381851038
Not applicable05907381850475
PRO0081905907381850741
Lipotris™05907381850796