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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

1 MHz Sonde, screwed, right side,… — Class IIa MDR

MD Atlas
Compumedics Germany GmbH

EUDAMED last updated this device on May 27, 2026

1 MHz Sonde, screwed, right side, green labeling

4260493316016VE

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Compumedics Germany GmbH
UDI-DI code: 04260493310246
Reference / catalog number: 7070

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Manufacturer information

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

Related devices

2 MHz Probe MRSafe, click&stay, orange labeling, 3 m)4260493316016VEOn the market 2 MHz Probe MRSafe, click&stay, orange labeling, 5 m)4260493316016VEOn the market 2 MHz Sonde, click&stay, left side, orange labeling4260493316016VEOn the market 4 MHz Probe, click&stay, right side, green labeling4260493316016VEOn the market 4 MHz Probe, screwed, left side, orange labeling4260493316016VEOn the market

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: 1 MHz Sonde, screwed, right side, green labeling
UDI-DI code: 04260493310246
Basic UDI-DI: 4260493316016VE
Reference / catalog number: 7070
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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Certificates

Certificate health across this manufacturer's portfolio.

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