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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

032-0-3000 — Class IIa MDR by gbo Medizintechnik AG

MD Atlas
gbo Medizintechnik AG

EUDAMED last updated this device on May 28, 2026

032-0-3000

426036481B010XH

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: gbo Medizintechnik AG
UDI-DI code: 04260364810103
Reference / catalog number: 032-0-3000

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View device family (Basic UDI)

Manufacturer information

Organization name: gbo Medizintechnik AG
SRN: DE-MF-000018065
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
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	May 28, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260364810103
Basic UDI-DI: 426036481B010XH
Reference / catalog number: 032-0-3000
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

UDI-DI DataMatrix

Encoded

(01)04260364810103

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z120610ULTRASOUND THERAPY EQUIPMENT

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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Related devices

033-0-1002/3B-04260364812152On the market 032-0-3100426036481B010XHOn the market 022-0-5000B-04260364811117On the market 020-0-5000B-04260364811124On the market 033-0-1002/2B-04260364812145On 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.