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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

WV0003 — Class I MDR by PS Product Services GmbH

MD Atlas
PS Product Services GmbH

EUDAMED last updated this device on Jun 25, 2025

WV0003

4050235PS0008BQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PS Product Services GmbH
UDI-DI code: 04050235004591
Reference / catalog number: WV0003

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Manufacturer information

Organization name: PS Product Services GmbH
SRN: DE-MF-000005290
Manufacturer status: Active

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FP00354050235PS0004BGOn the market FP00354050235PS0004BGOn the market FP00354050235PS0004BGOn the market FP00354050235PS0004BGOn the market FP00094050235PS0004BGOn the market

Critical warnings

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

CW999
Das Tape darf nicht auf oenen Wunden, verletzter Haut, Schleimhäuten, am Auge, in der Genitalzone, während der Schwangerschaft im Bauchbereich, bei sehr großen Ödemen und gleichzeitiger Herzerkrankung, bei Fieber, im Bereich von tiefen Venenthrombosen, Krampfadern oder Tumoren, bei Neurodermitis, Psoriasis (Schuppenflechte) und Hautausschlag angewendet werden. Nicht bei bekannter Überempndlichkeit gegenüber Acrylatkleber (Pflasterallergie) anwenden.
CW999
• Angelegte Tapes nicht länger als 5 Tage tragen. • Legen Sie das Tape so an, dass die Blutzirkulation nicht beeinträchtigt wird. • Tape nicht als Verbandsmaterial verwenden. • In sehr seltenen Fällen können lokale Überempndlichkeitsreaktionen auftreten, z. B. Juckreiz, Rötungen, Quaddelbildung. • Wenn Probleme beim Tragen auftreten, dann entfernen Sie das Tape sofort und kontaktieren Sie einen Arzt. • Schwerwiegende Vorfälle sind dem Hersteller und der zuständigen Behörde zu melden.

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: 04050235004591
Basic UDI-DI: 4050235PS0008BQ
Reference / catalog number: WV0003
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: 2
Additional product description: Physio Tape
Additional information URL: https://www.product-services.de/download/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - 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

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.