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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

Avevitta — Class I MDR by SANKOM SA

MD Atlas
SANKOM SA

EUDAMED last updated this device on Mar 3, 2026

Avevitta

76401259305420101A4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SANKOM SA
UDI-DI code: 07640125930344
Reference / catalog number: AVE-W01-AB-GR Grey Women Underwear XL

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Manufacturer information

Organization name: SANKOM SA
SRN: CH-MF-000047525
Manufacturer status: Active

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: Avevitta
UDI-DI code: 07640125930344
Basic UDI-DI: 76401259305420101A4
Reference / catalog number: AVE-W01-AB-GR Grey Women Underwear XL
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: The intended purpose of the Avevitta Underwear is to collect urine, and/or menstrual blood (for women). The devices are non-invasive, non-sterile, single-use disposable diapers to be used independently or in combination with a fixation pant.
Additional information URL: https://www.avevitta.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T04010103INCONTINENCE NAPPIES WITH INTEGRATED FIXING SYSTEM

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

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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.