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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

52598-003 — Class I MDR by biocon Medizintechnik…

MD Atlas
biocon Medizintechnik GmbH

EUDAMED last updated this device on Mar 26, 2026

52598-003

42514803047KX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: biocon Medizintechnik GmbH
UDI-DI code: 04251480317751
Reference / catalog number: 52598-003

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Manufacturer information

Organization name: biocon Medizintechnik GmbH
SRN: DE-MF-000006429
Manufacturer status: Active

Related devices

52598-00442514803047KXOn the market 52598-00142514803047KXOn the market 9220012042514803001K7On the market 9342212542514803001K7On the market 9145106042514803001K7On the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.
CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04251480317751
Basic UDI-DI: 42514803047KX
Reference / catalog number: 52598-003
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: 12
Additional product description: —
Additional information URL: https://biocon-online.de/downloads/2.2%206072-001%20Cliniflex%20Gebrauchanweisung%20Rev.%2004_10-2025.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A030499ADMINISTRATION KITS - 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

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.