Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

201110-1F — Class I MDR by Lentismed d.o.o.

MD Atlas
Lentismed d.o.o.

EUDAMED last updated this device on Feb 2, 2022

201110-1F

385889221stomaprodsSF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lentismed d.o.o.
UDI-DI code: 03858892215548
Reference / catalog number: 201110-1F

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

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: not provided
UDI-DI code: 03858892215548
Basic UDI-DI: 385889221stomaprodsSF
Reference / catalog number: 201110-1F
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: Bags for Ileostomy two piece open, flexible closure, small, transparent
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A10020301ILEOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O 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

Related devices

CompactCath Nelaton, Female, 10 Fr/Ch, 19cm385889221cathetersgelPAOn the market CompactCath Nelaton, Female, 12 Fr/Ch, 19cm385889221cathetersgelPAOn the market CompactCath Nelaton, Female, 14 Fr/Ch, 19cm385889221cathetersgelPAOn the market CompactCath Nelaton, Female, 16 Fr/Ch, 19cm385889221cathetersgelPAOn the market

CompactCath Nelaton, Female, 18 Fr/Ch, 19cm

385889221cathetersgelPA

On the market