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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

06766849 — Class I MDR by WQS Management…

MD Atlas
WQS Management Consultants GmbH

EUDAMED last updated this device on Jul 16, 2024

06766849

PP07484AMMOLA51

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: WQS Management Consultants GmbH
UDI-DI code: 110676684906
Reference / catalog number: 06766849

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Manufacturer information

Organization name: WQS Management Consultants GmbH
SRN: DE-MF-000005492
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW999
Reizt Augen, bei längerem Kontakt auch Atemorgane und Haut. Nur äußerlich anwenden. Nicht in die Augen bringen. Darf nicht in die Hände von Kindern gelangen. Nicht verwenden, wenn eine Überempfindlichkeit gegenüber einem der Inhaltsstoffe besteht. Darf nicht nach Ablauf des Verfallsdatums benutzt werden.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: 110676684906
Basic UDI-DI: PP07484AMMOLA51
Reference / catalog number: 06766849
Issuing entity: IFA

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.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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.