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Organization name
UDI-DI code
Reference / catalog number

79052 — Class I MDR by Friedrich Huber…

MD Atlas
Friedrich Huber aeronova GmbH & Co. KG

EUDAMED last updated this device on May 15, 2026

79052

4262437040Kaeltespray7X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Friedrich Huber aeronova GmbH & Co. KG
UDI-DI code: 04262437041056
Reference / catalog number: 79052

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Manufacturer information

Organization name: Friedrich Huber aeronova GmbH & Co. KG
SRN: DE-MF-000009163
Manufacturer status: Active

Related devices

790514262437040Kaeltespray7XOn the market 790504262437040Kaeltespray7XOn the market 790494262437040Kaeltespray7XOn the market 790484262437040Kaeltespray7XOn the market 790474262437040Kaeltespray7XOn 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 Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262437041056
Basic UDI-DI: 4262437040Kaeltespray7X
Reference / catalog number: 79052
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: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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
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Software identification