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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

FK10 — Class I MDR by DIA-MED Egészségügyi és…

MD Atlas
DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.

EUDAMED last updated this device on Jan 4, 2024

FK10

599957120FK00NJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.
UDI-DI code: 05999571200238
Reference / catalog number: FK10

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Manufacturer information

Organization name: DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.
SRN: HU-MF-000003115
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Hungary; available across 1 country total.

Country	On market since	Until
HungaryPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999571200238
Basic UDI-DI: 599957120FK00NJ
Reference / catalog number: FK10
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: https://www.dia-med.hu/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050101GENERIC USE STRETCHERS

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

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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.