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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

01236 — Class IIa MDD by intelligent motion GmbH

MD Atlas
intelligent motion GmbH

EUDAMED last updated this device on Apr 23, 2024

01236

B-09120125880019

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: intelligent motion GmbH
UDI-DI code: 09120125880019
Reference / catalog number: 01236

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Manufacturer information

Organization name: intelligent motion GmbH
SRN: AT-MF-000024765
Manufacturer status: Active

Critical warnings

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

CW016
EUDAMED did not publish a description for this code.
CW133
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09120125880019
Basic UDI-DI: B-09120125880019
Reference / catalog number: 01236
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: Roboter zur dreidimensionalen therapeutischen Bewegung von Patienten
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 0–165 MU29

EMDN nomenclature code(s)

Z120616ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPY

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

This device is not currently linked to any other device.

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.