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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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DIVA — 91 UDI-DI variants, MDR (NOBIL METAL SPA)

MD Atlas
NOBIL METAL SPA

Data from EUDAMED, last updated May 30, 2026

DIVA

8056039210306NM55DIVA0EX

91 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: NOBIL METAL SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8056039210306NM55DIVA0EX
Device name: DIVA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: NOBIL METAL SPA
SRN: IT-MF-000023048
Country: Italy
Email: contact@nobilmetal.it
Phone: +390141933811

Variants by status

UDI-DI variants

91 UDI-DI variants

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Applied filters

basicUdiUlid01KKKXC96PTRVEQ0GNG3HQH6HY

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

No registered UDI-DI variants for this device family.