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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

Carpex Comfort Type I — Class I MDR by Jahan Co. Unlimited…

MD Atlas
Jahan Co. Unlimited Company

EUDAMED last updated this device on May 18, 2026

Carpex Comfort Type I

539153673CMFT1CQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Jahan Co. Unlimited Company
UDI-DI code: 05391536730765
Reference / catalog number: 0906403

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Manufacturer information

Organization name: Jahan Co. Unlimited Company
SRN: IE-MF-000051008
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Ireland; available across 3 countries total.

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

Device identification

Trade name: Carpex Comfort Type I
UDI-DI code: 05391536730765
Basic UDI-DI: 539153673CMFT1CQ
Reference / catalog number: 0906403
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: 50
Additional product description: Carpex® is a registered trademark of Essity, distributed by BSN medical GmbH. Medical surgical face mask for single use, non-sterile, manufactured by Irema Ireland in accordance with EU standard EN 14683 for Type I performance. This product is the Carpex® Comfort model, which features a standard length nose bridge, making it the ideal standard mask for any user.
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

EMDN nomenclature code(s)

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

T020603MEDICAL USE FACE MASKS, TYPE I (NOT FOR HEALTHCARE PROFESSIONALS)

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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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.