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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

033-0-1002/2 — Class IIa MDD by gbo Medizintechnik AG

MD Atlas
gbo Medizintechnik AG

EUDAMED last updated this device on May 21, 2026

033-0-1002/2

B-04260364812145

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: gbo Medizintechnik AG
UDI-DI code: 04260364812145
Reference / catalog number: 033-0-1002/2

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Manufacturer information

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

Related devices

022-0-5000B-04260364811117On the market 020-0-5000B-04260364811124On the market 033-0-1100-02B-04260364811100On the market 58090010B-04260364811230On the market 033-0-1002B-04260364811193On the market

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	May 21, 2026	Dec 31, 2028
Austria	May 21, 2026	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 04260364812145
Basic UDI-DI: B-04260364812145
Reference / catalog number: 033-0-1002/2
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

EMDN nomenclature code(s)

Z120606MAGNETOTHERAPY 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.