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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 Products — 186 UDI-DI variants, MDR (Lentismed d.o.o.)

MD Atlas
Lentismed d.o.o.

Data from EUDAMED, last updated May 24, 2026

Ostomy Products

385889221stomaprodsSF

186 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: 385889221stomaprodsSF
Device name: Ostomy Products
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

186 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FQGQBKZBCC12JVV3RVQZYX1E

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

201140-103858892211625
LENTELL UroBag II XXS03858892217245
LENTELL UroBag II XXS; transparent03858892217962
201115-103858892214848
20111403858892214251
201114-103858892214817
20111303858892214244
201113-103858892214800
Lentell UroTouch Convex L03858892212356
Lentell UroTouch Convex S03858892212349
Lentell UroTouch Convex XL03858892216149

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