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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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PROIONIC® CREAMS — 2 UDI-DI variants, MDR (INDIBA S.A.U.)

MD Atlas
INDIBA S.A.U.

Data from EUDAMED, last updated May 23, 2026

PROIONIC® CREAMS

8434251A5D1D2Z0000ME

2 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: INDIBA S.A.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8434251A5D1D2Z0000ME
Device name: PROIONIC® CREAMS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: INDIBA S.A.U.
SRN: ES-MF-000001243
Country: Spain
Email: regulatory@indiba.com
Phone: +34 93 265 55 22

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KM0AXN227VNTG75KT04S3BEM

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

ACRE12108434251000380
IPC002508434251000403