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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

400-0003 — Class IIa MDR by Active Medical…

MD Atlas
Active Medical Xcellence GmbH

EUDAMED last updated this device on May 20, 2026

400-0003

4069019activeCut001VB

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Active Medical Xcellence GmbH
UDI-DI code: 04069019000049
Reference / catalog number: 400-0003

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Manufacturer information

Organization name: Active Medical Xcellence GmbH
SRN: DE-MF-000049306
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 Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04069019000049
Basic UDI-DI: 4069019activeCut001VB
Reference / catalog number: 400-0003
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: The MaCu Operation Kit 10 contains: - 1x activeBlade (UDI-DI: 04069019000025) - 10x activeCollect (UDI-DI: 04069019000032)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U0999UROGENITAL ENDOSCOPIC DEVICES - 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

11000014069019activeCut001VBOn the market 11000004069019activeCut001VBOn the market 10000004069019activeCut001VBOn the market 10000024069019activeCut001VBOn the market

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.