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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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Relizema cream — 5 UDI-DI variants, MDR (RELIFE S.r.l.)

MD Atlas
RELIFE S.r.l.

Data from EUDAMED, last updated May 30, 2026

Relizema cream

805534824RelizemaCreamJ9

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RELIFE S.r.l.

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 805534824RelizemaCreamJ9
Device name: Relizema cream
Device model: DLP011
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: RELIFE S.r.l.
SRN: IT-MF-000007611
Country: Italy
Email: contact@relifecompany.it
Phone: +3905556809345

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HFEGRKP9QGRCE2DPBW43X9PX

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

ZV036108055348240023
ZS034508055348240030
ZS034808055348240054
ZV036208055348240016
ZS034708055348240061