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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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SAMSON — 30 UDI-DI variants, MDR (SIGVARIS AG)

MD Atlas
SIGVARIS AG

Data from EUDAMED, last updated May 31, 2026

SAMSON

7611711SAMSONWE

30 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: SIGVARIS AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7611711SAMSONWE
Device name: —
Device model: SAMSON
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: SIGVARIS AG
SRN: CH-MF-000015565
Country: Switzerland
Email: ra.ssg@sigvaris.com
Phone: +41 71 272 40 00

Authorised representative

Name: Sigvaris GmbH
SRN: DE-AR-000010016
Country: Germany
Phone: +49 8331 757 0

Variants by status

UDI-DI variants

30 UDI-DI variants

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Applied filters

basicUdiUlid01KS7XTN2Q8PQ2YC4AC3S64HQK

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

SAMSON07611711976176
SAMSON07611711976121
SAMSON07611711976251
SAMSON07611711976268
SAMSON07611711976275

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