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

8040 — Class I MDR by Medicline društvo s…

MD Atlas
Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju

EUDAMED last updated this device on Feb 19, 2026

8040

385889598INCO0001H9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju
UDI-DI code: 03858895980054
Reference / catalog number: 8040

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: Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju
SRN: HR-MF-000048512
Manufacturer status: Active

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: 03858895980054
Basic UDI-DI: 385889598INCO0001H9
Reference / catalog number: 8040
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: Adult diapers for incontinence aid
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 130–160 MU10

EMDN nomenclature code(s)

T04010103INCONTINENCE NAPPIES WITH INTEGRATED FIXING SYSTEM

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

177177385889598INCO0001H9On the market 7030385889598INCO0001H9On the market 7050385889598INCO0001H9On the market 7040385889598INCO0001H9On the market 6030385889598INCO0001H9On the market

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.