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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

DE-0252 — Class IIa MDR by Dr. Pfleger…

MD Atlas
Dr. Pfleger Arzneimittel GmbH

EUDAMED last updated this device on Jan 28, 2025

DE-0252

PP22860LP191

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Pfleger Arzneimittel GmbH
UDI-DI code: 111916469003
Reference / catalog number: DE-0252

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Manufacturer information

Organization name: Dr. Pfleger Arzneimittel GmbH
SRN: DE-MF-000010172
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW999
Für Kinder unzugänglich aufbewahren!

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Nov 8, 2024	Still on market
Austria	Nov 8, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 111916469003
Basic UDI-DI: PP22860LP191
Reference / catalog number: DE-0252
Issuing entity: IFA

Classification

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

Device details

Quantity: 4
Additional product description: The intended purpose of ipalat Hydro Med® akut is to alleviate -the painful symptoms during irritation and inflammation of the mouth and throat (e.g. swelling, redness, sore throat,difficulty swallowing) - hoarseness, - tickle in the throat - dry mouth. They also protect the mucous membranes from further irritants.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

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

DE-0252PP22860LP191On 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.