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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

OBPOH — Class I MDR by Unikulma Oy

MD Atlas
Unikulma Oy

EUDAMED last updated this device on Jul 19, 2023

OBPOH

643002415OBAL46

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Unikulma Oy
UDI-DI code: 06430024154474
Reference / catalog number: OBPOH

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Manufacturer information

Organization name: Unikulma Oy
SRN: FI-MF-000035016
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Dec 5, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 06430024154474
Basic UDI-DI: 643002415OBAL46
Reference / catalog number: OBPOH
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: Ortobed pohjat ovat sähköisesti, joko langallisella tai langattomalla kaukosäätimellä säädettäviä, vuoteen runkoon asennettavia patja-alustoja. Ortobed pohjalla saadaan patja säädettyä moniin eri asentoihin, joilla saavutetaan useita suotuisia sekä lääketieteellisiä että terapeuttisia hyötyjä (ns. asentohoito). Ortobed pohja on suunnitelu lievittämään ja ehkäisemään tehokkaasti mm. kroonisia niska- ja selkäkipuja, ruoansulatusvaivoja, kuten närästystä sekä kuorsausta ja uniapneaa. Ortobed pohjan käyttö myös tehostaa palautumista fyysisestä rasituksesta parantamalla kehon aineenvaihduntaa.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS

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

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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.