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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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Delilah by Sigvaris transparent — 28 UDI-DI variants, MDR

MD Atlas
SIGVARIS SAS

Data from EUDAMED, last updated May 31, 2026

Delilah by Sigvaris transparent

361161DT52BS

28 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 SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 361161DT52BS
Device name: —
Device model: Delilah by Sigvaris transparent
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: SIGVARIS SAS
SRN: FR-MF-000023834
Country: France
Email: Affaires-Règlementaires@sigvaris.com

Variants by status

UDI-DI variants

28 UDI-DI variants

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Applied filters

basicUdiUlid01KSJ1192CN1TPDMV5YHR8FHAF

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

No registered UDI-DI variants for this device family.