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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

CEROTTO PROFUMATO PER… — Class I MDR by Air Note GmbH

MD Atlas
Air Note GmbH

EUDAMED last updated this device on Apr 21, 2023

CEROTTO PROFUMATO PER INCONTINENZA E STOMA

7640182560010AIRNOTEMP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Air Note GmbH
UDI-DI code: 76401825600650
Reference / catalog number: CEROTTO PROFUMATO PER INCONTINENZA E STOMA

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Manufacturer information

Organization name: Air Note GmbH
SRN: CH-MF-000034542
Manufacturer status: Active

Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 76401825600650
Basic UDI-DI: 7640182560010AIRNOTEMP
Reference / catalog number: CEROTTO PROFUMATO PER INCONTINENZA E STOMA
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: CEROTTO PROFUMATO DA NON APPLICARE DIRETTAMENTE SULLA PELLE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D99DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR MEDICAL DEVICES - 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

This device is not currently linked to any other device.

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.