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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

2+2.5 MHz Probe, click&stay, red… — Class IIa MDR

MD Atlas
Compumedics Germany GmbH

EUDAMED last updated this device on May 27, 2026

2+2.5 MHz Probe, click&stay, red labeling

4260493316016VE

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Compumedics Germany GmbH
UDI-DI code: 04260493310406
Reference / catalog number: 6034_1

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Manufacturer information

Organization name: Compumedics Germany GmbH
SRN: DE-MF-000005586
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

G10 054221 0016Issued
Quality management systemNotified body: 0123Expiry: Apr 3, 2028

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2000	Still on market

Device identification

Trade name: 2+2.5 MHz Probe, click&stay, red labeling
UDI-DI code: 04260493310406
Basic UDI-DI: 4260493316016VE
Reference / catalog number: 6034_1
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Z11040299ULTRASOUND PROBES – 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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