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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

get up 3200S — Class I MDR by Febromed GmbH & Co. KG

MD Atlas
Febromed GmbH & Co. KG

EUDAMED last updated this device on Nov 27, 2023

get up 3200S

426074055GETUP86

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Febromed GmbH & Co. KG
UDI-DI code: 04260740550258
Reference / catalog number: get up 3200S

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Manufacturer information

Organization name: Febromed GmbH & Co. KG
SRN: DE-MF-000009287
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW010
Healthcare professional must read the instructional manuel completely before use the get up for the first time.
CW030
Do not use without a healthcare professional
CW011
Material damaged by overload

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: 04260740550258
Basic UDI-DI: 426074055GETUP86
Reference / catalog number: get up 3200S
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: Das get up ist eine schwenkbare Aufrichthilfe. An dem Schwenkarm hängt ein Triangelgriff, an dem sich der Patient während der Besteigung einer Behandlungseinheit festhalten kann.
Additional information URL: https://www.febromed.de/get-up/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050399PATIENT TRANSFER LIFTS - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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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.