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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

ATL-A-7D001 — Class I MDR by ATLAS medical…

MD Atlas
ATLAS medical technologies GmbH

EUDAMED last updated this device on Oct 28, 2025

ATL-A-7D001

++G083ATLA7DWS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ATLAS medical technologies GmbH
UDI-DI code: *+G083ATLA7D0010/$$+7240906-01$*
Reference / catalog number: ATL-A-7D001

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Manufacturer information

Organization name: ATLAS medical technologies GmbH
SRN: DE-MF-000024705
Manufacturer status: Active

Related devices

ATL-D-PA001ns++G083ATLDPA00154On the market ATL-D-PT002ns++G083ATLDPTNS96On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: *+G083ATLA7D0010/$$+7240906-01$*
Basic UDI-DI: ++G083ATLA7DWS
Reference / catalog number: ATL-A-7D001
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: The Laser Robot Arm is an electromechanical arm designed to provide visual guidance to physicians for the manual positioning and advancement of rigid, straight instruments such as needles, during image-guided percutaneous procedures.Th LRA is intended for use in minimally invasive procedures, including periradicular therapy, and is compatible with computed tomography (CT) imaging.
Additional information URL: https://atlas4d.de/products-services/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011401SURGICAL NAVIGATION SYSTEM

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.