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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

SAN-055CPC Peach L-XL — Class I MDR by SANKOM SA

MD Atlas
SANKOM SA

EUDAMED last updated this device on Apr 29, 2025

SAN-055CPC Peach L-XL

7640125930550101AZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SANKOM SA
UDI-DI code: 07640125935042
Reference / catalog number: SAN-055CPC Peach L-XL

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Manufacturer information

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

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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: 07640125935042
Basic UDI-DI: 7640125930550101AZ
Reference / catalog number: SAN-055CPC Peach L-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: Multilevel targeted anatomical compression and shaping effect of the SANKOM Shaper enhances the silhouette and creates a beautiful figure as it lifts the butt, flattens stomach, defines waist and slims thighs It is a perfect undergarment for a post-pregnancy period since it helps to restore the body both physiologically and esthetically Patented diagonal compression readjusts the body's center of gravity into its correct position, therfore, decreases the load on spine
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.