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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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Organization name
UDI-DI code
Reference / catalog number

MExT Noseblot — Class I MDR by Mondomed NV

MD Atlas
Mondomed NV

EUDAMED last updated this device on Aug 18, 2025

MExT Noseblot

542502543ENTEK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mondomed NV
UDI-DI code: 05425025439355
Reference / catalog number: 1155500M

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View device family (Basic UDI)

Manufacturer information

Organization name: Mondomed NV
SRN: BE-MF-000001283
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

BE24/00000069Issued
Quality management systemNotified body: 1639Expiry: Mar 8, 2029

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Belgium; available across 1 country total.

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

Device identification

Trade name: MExT Noseblot
UDI-DI code: 05425025439355
Basic UDI-DI: 542502543ENTEK
Reference / catalog number: 1155500M
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: 3
Additional product description: Absorbent nasal plug 45x20 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05425025439355

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q030299EPISTAXIS DEVICES - OTHER

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

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