Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

SAN-091TBG Beige L-XL — Class I MDR by SANKOM SA

MD Atlas
SANKOM SA

EUDAMED last updated this device on Oct 26, 2025

SAN-091TBG Beige L-XL

7640125930910102BB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SANKOM SA
UDI-DI code: 07640125934731
Reference / catalog number: SAN-091TBG Beige L-XL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

Avevitta76401259305420101A4On the market Avevitta76401259305420101A4On the market Avevitta76401259305420101A4On the market Avevitta76401259305420101A4On the market Avevitta76401259305420101A4On the market

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 Poland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 07640125934731
Basic UDI-DI: 7640125930910102BB
Reference / catalog number: SAN-091TBG Beige 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: A compression tights that help the blood circulation at the same time that is supporting the lower back
Additional information URL: https://www.sankom.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030405COMPRESSION STOCKINGS

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