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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

18.2200 — Class I MDR by Rehadapt GmbH

MD Atlas
Rehadapt GmbH

EUDAMED last updated this device on Jan 13, 2022

18.2200

++B896KeyguardsVW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rehadapt GmbH
UDI-DI code: +B89618220002
Reference / catalog number: 18.2200

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Manufacturer information

Organization name: Rehadapt GmbH
SRN: DE-MF-000008141
Manufacturer status: Active

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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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 31, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: +B89618220002
Basic UDI-DI: ++B896KeyguardsVW
Reference / catalog number: 18.2200
Issuing entity: HIBCC

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: Keyguards: for the iPad 10.2" in a AMDI iAdapter 10 case for the Predictable 5 software. Grid: QWERTZ with Message Bar. Mounting Kit Flex Band 100 included.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y214299DEVICES FOR INTERPERSONAL COMUNICATION - 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

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Expiration date
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Software identification