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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

01 — Class I MDR by Augmedit B.V.

MD Atlas
Augmedit B.V.

EUDAMED last updated this device on Mar 3, 2026

01

87208926176LumiCFEM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Augmedit B.V.
UDI-DI code: 08720892617644
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

Related devices

0187208926176LumiPrepareQNOn the market Lumi Referenced87208926176LumiRef8JOn the market 0187208926176LumiSegmentN7On the market

Certificates

Certificate health across this manufacturer's portfolio.

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

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08720892617644
Basic UDI-DI: 87208926176LumiCFEM
Reference / catalog number: 01
Issuing entity: GS1

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: This is an accessory to Lumi Prepare (87208926176LumiPrepareQN) and Lumi Segment (87208926176LumiSegmentN7)
Additional information URL: No additional information URL provided by the manufacturer.
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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