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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

1931101 — Class I MDR by HERBOLIVA 10 S.L.

MD Atlas
HERBOLIVA 10 S.L.

EUDAMED last updated this device on Feb 2, 2026

1931101

8437015720OLEICOPIELDZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HERBOLIVA 10 S.L.
UDI-DI code: 08437015720104
Reference / catalog number: 1931101

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Manufacturer information

Organization name: HERBOLIVA 10 S.L.
SRN: ES-MF-000038660
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
- Mantener fuera del alcance de los niños. - Uso Externo. No ingerir. - No masajear, ni frotar la piel para evitar dañarla. - En caso de lesiones o ulcera en la piel, dejar de usar el producto y tratar la lesión. - En caso de alergias en la piel dejar de usar el producto y consultar con un profesional sanitario.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08437015720104
Basic UDI-DI: 8437015720OLEICOPIELDZ
Reference / catalog number: 1931101
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: SOLUCIÓN TÓPICA
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M04041501DRESSINGS IN SOLUTIONS, EMULSIONS, GELS, POWDERS WITH HERBAL COMPONENTS

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

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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.