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

Sparadrap doigt (6x4cm) — Class I MDR by M.Ex.T. Belgium

MD Atlas
M.Ex.T. Belgium

EUDAMED last updated this device on Mar 25, 2026

Sparadrap doigt (6x4cm)

54009380001-WDKY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M.Ex.T. Belgium
UDI-DI code: 05400938000847
Reference / catalog number: 0020.922

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: M.Ex.T. Belgium
SRN: BE-MF-000022927
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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW007
Do not use if package is damaged

Market distribution

Primary placement in Belgium; available across 3 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
Germany		Still on market
Netherlands		Still on market

Device identification

Trade name: Sparadrap doigt (6x4cm)
UDI-DI code: 05400938000847
Basic UDI-DI: 54009380001-WDKY
Reference / catalog number: 0020.922
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: 6
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M04010102POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD

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

Adhesive plaster blue, 0,02x5m54009380002-PLL2On the market Adhesive plaster silk, 0,0125x5m54009380002-PLL2On the market Adhesive plaster silk, 0,0250x5m54009380002-PLL2On the market Cohesive Bandage, 0,08x4m54009380003-BAJ9On the market Cohesive Bandage, 2,5cmx4m54009380003-BAJ9

On the market