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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

Lumi Referenced — Class IIb MDR by Augmedit B.V.

MD Atlas
Augmedit B.V.

EUDAMED last updated this device on Jan 16, 2026

Lumi Referenced

87208926176LumiRef8J

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Augmedit B.V.
UDI-DI code: 08720892617620
Reference / catalog number: 01

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View device family (Basic UDI)

Manufacturer information

Organization name: Augmedit B.V.
SRN: NL-MF-000045948
Manufacturer status: Active

Critical warnings

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

CW011
• In case of device failure, immediately disconnect and contact technical support of Augmedit B.V.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Jan 1, 2026	Still on market

Device identification

Trade name: Lumi Referenced
UDI-DI code: 08720892617620
Basic UDI-DI: 87208926176LumiRef8J
Reference / catalog number: 01
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://lumi.cloud/LumiReferenced_InstructionsForUse.pdf
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z11069092VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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

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Related devices

0187208926176LumiPrepareQNOn the market 0187208926176LumiSegmentN7On the market 0187208926176LumiCFEMOn the market

Certificates

Certificate health across this manufacturer's portfolio.

SCAR-8.2.1.4Amended
Quality management systemNotified body: 3022Expiry: Oct 6, 2030