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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

G4.12.23 — Class I MDR by BRUMABA GmbH

MD Atlas
BRUMABA GmbH

EUDAMED last updated this device on May 22, 2023

G4.12.23

42602477713-961DA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BRUMABA GmbH
UDI-DI code: 04260247770241
Reference / catalog number: G4.12.23

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Manufacturer information

Organization name: BRUMABA GmbH
SRN: DE-MF-000006236
Manufacturer status: Active

Related devices

G4.01.2342602477713-961DAOn the market G4.11.2342602477713-961DAOn the market G4.01.1242602477713-961DAOn the market G4.11.1242602477713-961DAOn the market Y1.01.2342602477713-961DAOn the market

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260247770241
Basic UDI-DI: 42602477713-961DA
Reference / catalog number: G4.12.23
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: BRUMABA Operating Table is a comfortable and versatile operating table, which can be hydraulically adjusted to the required position using the manual control or the foot control. The patient can be positioned appropriately and automatically thanks to the division of the table top.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011202OPERATING TABLES

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.