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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

Crachoir blanc — Class I MDR by OLFA

MD Atlas
OLFA

EUDAMED last updated this device on Feb 18, 2026

Crachoir blanc

3155535051006R

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OLFA
UDI-DI code: 03155535051007
Reference / catalog number: 6505100

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Manufacturer information

Organization name: OLFA
SRN: FR-MF-000010359
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.
CW011
Livré non stérile. Lavage requis avant première utilisation. Lavage impératif entre chaque utilisation. Ce produit est un dispositif médical destiné à un usage professionnel.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: Crachoir blanc
UDI-DI code: 03155535051007
Basic UDI-DI: 3155535051006R
Reference / catalog number: 6505100
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: Récipient hygiénique pour recueillir la salive ou le mucus qui encombrent les voies respiratoires et les bronches. Produit pré-monté avec son couvercle. Couvercle doté d'un levier d'ouverture pouce strié (système anti-glisse).
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0402CLINICAL USE TRAYS AND BOWLS

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.