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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

KB50 250AB — Class I MDR by Kajo Apuvälineet Oy

MD Atlas
Kajo Apuvälineet Oy

EUDAMED last updated this device on May 9, 2022

KB50 250AB

6429810721KajoButtonUD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kajo Apuvälineet Oy
UDI-DI code: 06429810721136
Reference / catalog number: KB50 250AB

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Manufacturer information

Organization name: Kajo Apuvälineet Oy
SRN: FI-MF-000002471
Manufacturer status: Active

Related devices

Kajo106429810721Kajo10S7On the market KB100 250CR6429810721KajoButtonUDOn the market KB100 250CB6429810721KajoButtonUDOn the market KB25 150BB6429810721KajoButtonUDOn the market KB25 250 BB6429810721KajoButtonUDOn the market

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.

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: 06429810721136
Basic UDI-DI: 6429810721KajoButtonUD
Reference / catalog number: KB50 250AB
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: KajoButton50, sensitivity: 250 g cable length: 25 cm color: black
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y240999CONTROL DEVICES AND SYSTEMS - 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

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Expiration date
Manufacturing date
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Software identification