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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

C1.02.13 — Class I MDR by BRUMABA GmbH

MD Atlas
BRUMABA GmbH

EUDAMED last updated this device on May 17, 2023

C1.02.13

42602477718-139DY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BRUMABA GmbH
UDI-DI code: 04260247770081
Reference / catalog number: C1.02.13

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Manufacturer information

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

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.

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: 04260247770081
Basic UDI-DI: 42602477718-139DY
Reference / catalog number: C1.02.13
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: Ein rein mechanischer Patienten Transportstuhl, der sowohl in eine Sitz- als auch Liegeposition eingestellt werden kann.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019010PATIENT TRANSFER SYSTEMS

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

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Expiration date
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