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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

03003133 — Class I MDR by Deutsche Olbas GmbH

MD Atlas
Deutsche Olbas GmbH

EUDAMED last updated this device on Feb 11, 2026

03003133

40063093132GK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Deutsche Olbas GmbH
UDI-DI code: 04006309031338
Reference / catalog number: 03003133

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Manufacturer information

Organization name: Deutsche Olbas GmbH
SRN: DE-MF-000017839
Manufacturer status: Active

Critical warnings

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

CW055
Extrem entzündbares Aerosol.
CW268
Kann bei Erwärmung bersten.
CW139
Von Hitze/Funken/offener Flamme/heißen Oberflächen fernhalten
CW140
Nicht in offene Flamme oder andere Zündquellen sprühen.
CW157
Behälter steht unter Druck: nicht durchstechen oder verbrennen, auch nicht nach der Verwendung.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04006309031338
Basic UDI-DI: 40063093132GK
Reference / catalog number: 03003133
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: label
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M9001CRYOTHERAPY AND THERMOTHERAPY 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.