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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

95120LL — Class I MDR by Suomen Sairaalatukku Oy

MD Atlas
Suomen Sairaalatukku Oy

EUDAMED last updated this device on Dec 1, 2023

95120LL

642981091595120LLSSTQA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Suomen Sairaalatukku Oy
UDI-DI code: 06429810915016
Reference / catalog number: 95120LL

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Manufacturer information

Organization name: Suomen Sairaalatukku Oy
SRN: FI-MF-000038334
Manufacturer status: Active

Critical warnings

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

CW018
Vasta-aiheet vuodesuoja ei sovellu bariatrisille potilaille, koska laitteen suunniteltu kantavuus on max.250kg. Lisäksi laitetta ei ole tarkoitettu koneelliseen nostoon, manuaalisen noston apuvälineeksi ja pestäväksi huuhteluaineella. Varoitus: huuhteluaineen tai valkaisuaineen käyttö haurastuttaa tuotteen vinyylikerrosta ja tuote voi päästää nesteitä läpi. Tuotteen kuivaaminen pesuohjeen vastaisesti aiheuttaa suojan sisällä olevien muovikalvojen sulamisen ja vuodesuojan muuttumisen ryppyiseksi.

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 06429810915016
Basic UDI-DI: 642981091595120LLSSTQA
Reference / catalog number: 95120LL
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 95x120 cm

EMDN nomenclature code(s)

T04010299ABSORBENT UNDERPADS - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.