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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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DIGIPORT — 4 UDI-DI variants, MDR (NEW LIFE RADIOLOGY Srl)

MD Atlas
NEW LIFE RADIOLOGY Srl

Data from EUDAMED, last updated May 31, 2026

DIGIPORT

803367560DIGIPORTYR

4 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: NEW LIFE RADIOLOGY Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803367560DIGIPORTYR
Device name: DIGIPORT
Device model: DIGIPORT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEW LIFE RADIOLOGY Srl
SRN: IT-MF-000044708
Country: Italy
Email: obadawnehnew@newliferadiology.it
Phone: +393336883850

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K4FT3DGHT7VQARJTK4T5SYZV

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

ENDOPORT-G08033675601182
ENDOPORT-C08033675601175
DIGIPORT-G08033675601168
DIGIPORT-C08033675601151