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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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SISSEL® PUTTY ivory flex — 5 UDI-DI variants, MDR (SISSEL GmbH)

MD Atlas
SISSEL GmbH

Data from EUDAMED, last updated May 23, 2026

SISSEL® PUTTY ivory flex

42506947Y0503CQ

5 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: SISSEL GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42506947Y0503CQ
Device name: SISSEL® PUTTY ivory flex
Device model: SISSEL® PUTTY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: SISSEL GmbH
SRN: DE-MF-000007624
Country: Germany
Email: info@sissel.de
Phone: +496322989430

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GYYAJXBHQTZJTRTSCSASF0EJ

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

162.01904250694711478
162.01804250694711447
162.01504250694711355
162.01704250694711416
162.01604250694711386