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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

601920 — Class I MDR by Laboratorium Dr. Deppe…

MD Atlas
Laboratorium Dr. Deppe GmbH

EUDAMED last updated this device on May 27, 2026

601920

4260181255127SN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorium Dr. Deppe GmbH
UDI-DI code: 04260181256726
Reference / catalog number: 601920

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View device family (Basic UDI)

Manufacturer information

Organization name: Laboratorium Dr. Deppe GmbH
SRN: DE-MF-000005103
Manufacturer status: Active

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Critical warnings

8 warnings recorded — scroll inside the panel to see all entries.

CW041
Gefahr
CW045
Umweltgefährdend
CW104
Sehr giftig für Wasserorganismen, mit langfristiger Wirkung.
CW076
Gesundheitsschädlich bei Verschlucken.
CW102
Kann die Organe schädigen bei längerer oder wiederholter Exposition.
CW043
Achtung
CW044
Gefahr
CW081
Verursacht schwere Verätzungen der Haut und schwere Augenschäden.

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260181256726
Basic UDI-DI: 4260181255127SN
Reference / catalog number: 601920
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: —
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

UDI-DI DataMatrix

Encoded

(01)04260181256726

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

D0801ENZYMATIC DETERGENTS FOR MEDICAL DEVICES

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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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.