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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

00019230 — Class IIb MDR by Dr. August Wolff GmbH &…

MD Atlas
Dr. August Wolff GmbH & Co. KG Arzneimittel

EUDAMED last updated this device on Mar 26, 2026

00019230

404888219230D3

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. August Wolff GmbH & Co. KG Arzneimittel
UDI-DI code: 04048882192303
Reference / catalog number: 00019230

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Manufacturer information

Organization name: Dr. August Wolff GmbH & Co. KG Arzneimittel
SRN: DE-MF-000005943
Manufacturer status: Active

Critical warnings

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

CW135
EUDAMED did not publish a description for this code.
CW999
Den Applikator aus Vorsicht in der Schwangerschaft nicht verwenden.
CW999
Nicht anwenden bei Überempfindlichkeit gegenüber einem der Bestandteile.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Dec 1, 2023	Still on market
Austria	Dec 1, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04048882192303
Basic UDI-DI: 404888219230D3
Reference / catalog number: 00019230
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 50g cream. Language: German
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U0803VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS

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

00012047404888212047BROn the market 00019281404888219281DLOn the market 00019273404888219273DMOn the market 00019738404888219737EAOn 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.