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Organization name
UDI-DI code
Reference / catalog number

HIMR0150 — Class I MDR by RIVIERA Pharma &…

MD Atlas
RIVIERA Pharma & Cosmetics GmbH

EUDAMED last updated this device on May 13, 2026

HIMR0150

9002757HIMR2U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RIVIERA Pharma & Cosmetics GmbH
UDI-DI code: 09002757015222
Reference / catalog number: HIMR0150

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Manufacturer information

Organization name: RIVIERA Pharma & Cosmetics GmbH
SRN: AT-MF-000004107
Manufacturer status: Active

Related devices

CIMR01509002757CIMRZNOn the market CMGG00259002757CMGGZ2On the market CMGG00759002757CMGGZ2On the market CMGG0500D9002757CMGGZ2On the market CMGG0500S9002757CMGGZ2On 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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW999
Nur zur äußerlichen Anwendung. Nur auf intakte Haut bringen. Nach dem Auftragen die Haut nicht dicht abdecken. Nach der Anwendung kann es zu lokalen Hautrötungen und einem intensiven Wärmegefühl kommen. Nicht für Kinder verwenden und Augenkontakt unbedingt vermeiden. Nicht auf Schleimhäuten und in der Nähe der Augen anwenden. Während der Schwangerschaft und Stillzeit nur nach ärztlicher Rücksprache anwenden.

Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09002757015222
Basic UDI-DI: 9002757HIMR2U
Reference / catalog number: HIMR0150
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: —
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