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UDI-DI code
Reference / catalog number

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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

N/A — Class IIa MDR by Kiro

MD Atlas
Kiro

Manufacturer information

Organization name: Kiro
SRN: FR-MF-000013869
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

C598485Issued
Quality management systemNotified body: 2460Expiry: Jun 14, 2030

Related devices

This device is not currently linked to any other device.

EUDAMED last updated this device on Jan 29, 2026

N/A

3770027838BEYOND9B

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kiro
UDI-DI code: 03770027838005
Reference / catalog number: N/A

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Manufacturer information

Organization name: Kiro
SRN: FR-MF-000013869
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Feb 14, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03770027838005
Basic UDI-DI: 3770027838BEYOND9B
Reference / catalog number: N/A
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: BEYOND is a software intended to help healthcare professionals with their diagnoses and patient care by providing recommendations based on medical exams and clinical data.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

C598485Issued
Quality management systemNotified body: 2460Expiry: Jun 14, 2030