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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

Caleçon à usage unique… — Class I MDR by AMBITION

MD Atlas
AMBITION

EUDAMED last updated this device on Jun 23, 2023

Caleçon à usage unique polypropylène 40g bleu foncé

3770023808CBF40Q3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AMBITION
UDI-DI code: 03770023808187
Reference / catalog number: CBF40

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Manufacturer information

Organization name: AMBITION
SRN: FR-MF-000034559
Manufacturer status: Active

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

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: Caleçon à usage unique polypropylène 40g bleu foncé
UDI-DI code: 03770023808187
Basic UDI-DI: 3770023808CBF40Q3
Reference / catalog number: CBF40
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: Le caleçon à usage unique est un sous-vêtement pratique permettant de maintenir une bonne hygiène aux patients/clients des professionnels de santé et de bien être lors de soins, séances de massages, séances d’épilation…. Secteur d’utilisation : santé / cliniques / hôpitaux / instituts de beauté et SPAS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0399PROTECTION DEVICES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT PPE) - 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

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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.