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Organization name
UDI-DI code
Reference / catalog number

Lentell IleoTouch Convex L — Class I MDR by Lentismed d.o.o.

MD Atlas
Lentismed d.o.o.

EUDAMED last updated this device on Sep 26, 2022

Lentell IleoTouch Convex L

385889221stomaprodsSF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lentismed d.o.o.
UDI-DI code: 03858892212325
Reference / catalog number: 201146L

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Manufacturer information

Organization name: Lentismed d.o.o.
SRN: HR-MF-000018298
Manufacturer status: Active

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Market distribution

Primary placement in Croatia; available across 1 country total.

Placed on the market in Croatia; per-country availability dates not published.

Device identification

Trade name: Lentell IleoTouch Convex L
UDI-DI code: 03858892212325
Basic UDI-DI: 385889221stomaprodsSF
Reference / catalog number: 201146L
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Lentell IleoTouch Convex Large
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A1001020202ONE-PIECE ILEOSTOMY BAGS FOR RETRACTED STOMA, CONVEX, WITH TISSUE COVER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

M.2022.MDR.1008Issued
Quality assuranceNotified body: 2696Expiry: Dec 11, 2027