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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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Premium Care — 12 UDI-DI variants, MDR (Nunex Worldwide, SA)

MD Atlas
Nunex Worldwide, SA

Data from EUDAMED, last updated May 31, 2026

Premium Care

560728370QB

12 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: Nunex Worldwide, SA

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 560728370QB
Device name: Premium Care
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nunex Worldwide, SA
SRN: PT-MF-000048317
Country: Portugal
Email: info@nunex.pt

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7G7X6XJ86DFHJF24DNX4DQ

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

NNX70366305607283703663
NNX70361805607283703618
NNX70365605607283703656
13.230000105607283703915
NNX70392205607283703922
NNX0181205607283701812
NNX70163805607283701638
NNX70265905607283702659
NNX70290105607283702901
NNX70295605607283702956
NNX70182905607283701829
NNX70186705607283701867