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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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MEDPLAST BANDA ADEZIVA — 4 UDI-DI variants, MDR (SC MEBRA SRL)

MD Atlas
SC MEBRA SRL

Data from EUDAMED, last updated May 30, 2026

MEDPLAST BANDA ADEZIVA

5944737medplastG8

4 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: SC MEBRA SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5944737medplastG8
Device name: MEDPLAST BANDA ADEZIVA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: SC MEBRA SRL
SRN: RO-MF-000017978
Country: Romania
Email: regulatory.mebra@gmail.com
Phone: +40268420146

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HZPQAKK17MBYP50G0CMMF56X

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

6179312505944737000177
6179320505944737000092
6179200505944737000184
6179100505944737000061