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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

06.3818.10M — Class III MDD by ACTO GmbH

MD Atlas
ACTO GmbH

EUDAMED last updated this device on Apr 27, 2026

06.3818.10M

B-04250108338161

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ACTO GmbH
UDI-DI code: 04250108338161
Reference / catalog number: 06.3818.10M

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Manufacturer information

Organization name: ACTO GmbH
SRN: DE-MF-000019128
Manufacturer status: Active

Related devices

06.3798.10M5B-05906190437143On the market 06.3818.10B-04250108338154On the market 06.3818.100B-04250108338130On the market 06.3818.05MB-04250108338178On the market 06.3818.30B-04250108338185On the market

Market distribution

Primary placement in Germany; available across 2 countries total.

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

Device identification

Trade name: not provided
UDI-DI code: 04250108338161
Basic UDI-DI: B-04250108338161
Reference / catalog number: 06.3818.10M
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M040412ANTISEPTICS-BASED DRESSINGS

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.