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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

02.1016.2 — Class IIb MDD by ACTO GmbH

MD Atlas
ACTO GmbH

EUDAMED last updated this device on May 21, 2026

02.1016.2

B-04250108310204

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ACTO GmbH
UDI-DI code: 04250108310204
Reference / catalog number: 02.1016.2

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Manufacturer information

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

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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

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.

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: 04250108310204
Basic UDI-DI: B-04250108310204
Reference / catalog number: 02.1016.2
Issuing entity: GS1

Classification

Risk category: Class IIb
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)

D0899DETERGENTS FOR MEDICAL 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