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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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CHILI PACS — 9 UDI-DI variants, MDR (NEXUS / CHILI GmbH)

MD Atlas
NEXUS / CHILI GmbH

Data from EUDAMED, last updated May 23, 2026

CHILI PACS

4260456230000T5

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: NEXUS / CHILI GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4260456230000T5
Device name: CHILI PACS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 10, 2021

Manufacturer & authorised representative

Manufacturer

Name: NEXUS / CHILI GmbH
SRN: DE-MF-000007503
Country: Germany
Email: info@nexus-chili.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJCBJYP5AWDP72AE9GF4T4CR

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

4.82.004260456230154
4.92.004260456230208
4.84.004260456230161
4.86.004260456230178
4.80.004260456230147
4.90.004260456230192
4.88.004260456230185
4.76.004260456230123
4.78.004260456230130