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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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T-LysYal® Crema Proctologica — 1 UDI-DI variant, MDR

MD Atlas
SILDEHA Pharma Srl

Data from EUDAMED, last updated May 31, 2026

T-LysYal® Crema Proctologica

805720449TLYSCREPRO2R

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: SILDEHA Pharma Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805720449TLYSCREPRO2R
Device name: T-LysYal® Crema Proctologica
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: SILDEHA Pharma Srl
SRN: IT-MF-000026622
Country: Italy
Email: infosildeha@sildeha.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KN4R89B6QBQVZPCT3WNQWYHQ

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

0SLD700C2G08057204490139