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Organization name
UDI-DI code
Reference / catalog number

SAN-071CBL Black XL-XXL — Class I MDR by SANKOM SA

MD Atlas
SANKOM SA

EUDAMED last updated this device on Apr 25, 2025

SAN-071CBL Black XL-XXL

7640125930710302AT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SANKOM SA
UDI-DI code: 07640125932201
Reference / catalog number: SAN-071CBL Black XL-XXL

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Manufacturer information

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

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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.

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: 07640125932201
Basic UDI-DI: 7640125930710302AT
Reference / catalog number: SAN-071CBL Black XL-XXL
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 SANKOM Bra pushes the shoulders backward and straightens the back, using the natural weight of the breasts Unlike other bras, it is made out of 2 individual structures giving each breast the support it needs as well as a push-up effect
Additional information URL: https://www.sankom.com/collections/shapewear
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - 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

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Expiration date
Manufacturing date
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Software identification