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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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Ostomy Accessories — 16 UDI-DI variants, MDR (Lentismed d.o.o.)

MD Atlas
Lentismed d.o.o.

Data from EUDAMED, last updated May 24, 2026

Ostomy Accessories

385889221stomaaccssHJ

16 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: Lentismed d.o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889221stomaaccssHJ
Device name: Ostomy Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 22, 2021

Manufacturer & authorised representative

Manufacturer

Name: Lentismed d.o.o.
SRN: HR-MF-000018298
Country: Croatia
Email: lentismed@lentismed.com
Phone: +385 1 558 4259

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FQH8K1TFSDABXP6VP0JYSG65

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

LENTELL Drainage pouch clamp03858892214527
20113403858892215067
20113103858892215036
201131W03858892219829
201131W03858892219829
20113203858892215043
20112803858892215005
20112903858892215012
Lentell OstoProtect03858892219768
20113003858892215029
LENTELL OstoProtect Swab03858892216644
201130W03858892219805
201130W03858892219805
Lentell OstoStrip03858892212226
20113503858892215074
20113603858892215081