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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

43739 — Class I MDR by Tjugohundra18 AB

MD Atlas
Tjugohundra18 AB

EUDAMED last updated this device on Apr 5, 2026

43739

734018574373901K2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tjugohundra18 AB
UDI-DI code: 07340185700139
Reference / catalog number: 43739

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View device family (Basic UDI)

Manufacturer information

Organization name: Tjugohundra18 AB
SRN: SE-MF-000003776
Manufacturer status: Active

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Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07340185700139
Basic UDI-DI: 734018574373901K2
Reference / catalog number: 43739
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: ProSense Antihalkstrumpa är en svart/grafitgrå strumpa designade med ett finmönstrat antihalkmönster som är bekvämt för känsliga fotsulor. Fallolyckor är vanligt och ett par antihalkstrumpor gör att du går säkrare och risken för att ramla minskar. ProSense strumpor är en unisex-modell och passar alla fötter. ProSense Antihalkstrumpor är tunna och kan därför kombineras med kompressions- och stödstrumpor om så önskas.
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.

Y0999PERSONAL CARE AIDS - 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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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.