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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

2371 — Class IIb MDD by Intermedt Medizin &…

MD Atlas
Intermedt Medizin & Technik GmbH

EUDAMED last updated this device on May 22, 2026

2371

B-42607708225542

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Intermedt Medizin & Technik GmbH
UDI-DI code: 42607708225542
Reference / catalog number: 2371

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View device family (Basic UDI)

Manufacturer information

Organization name: Intermedt Medizin & Technik GmbH
SRN: DE-MF-000006369
Manufacturer status: Active

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Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW018
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 5, 2006	Still on market

Device identification

Trade name: not provided
UDI-DI code: 42607708225542
Basic UDI-DI: B-42607708225542
Reference / catalog number: 2371
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC 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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)42607708225542

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

F0499DIALYSIS CONCENTRATES - 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

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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.