Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

HMGG0500D — Class I MDR by RIVIERA Pharma &…

MD Atlas
RIVIERA Pharma & Cosmetics GmbH

EUDAMED last updated this device on May 13, 2026

HMGG0500D

9002757HMGG28

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RIVIERA Pharma & Cosmetics GmbH
UDI-DI code: 09002757015321
Reference / catalog number: HMGG0500D

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: RIVIERA Pharma & Cosmetics GmbH
SRN: AT-MF-000004107
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
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 kommen. Nicht für Kinder unter 6 Jahren verwenden und Augenkontakt unbedingt vermeiden. Bei Kontakt mit den Augen: sofort gründlich mit reichlich Wasser ausspülen. Bei anhaltender Reizung einen Arzt konsultieren. Nicht auf Schleimhäuten und in der Nähe der Augen anwenden. Außerhalb der Reichweite von Kindern aufbewahren. 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: 09002757015321
Basic UDI-DI: 9002757HMGG28
Reference / catalog number: HMGG0500D
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

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.