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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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Reusable parts of biopsy system — 2 UDI-DI variants, MDR (Neonavia AB)

MD Atlas
Neonavia AB

Data from EUDAMED, last updated May 30, 2026

Reusable parts of biopsy system

735008194NEONAVIAREUSEDE

2 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: Neonavia AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735008194NEONAVIAREUSEDE
Device name: Reusable parts of biopsy system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: Neonavia AB
SRN: SE-MF-000045971
Country: Sweden
Email: magnus.olsen@neonavia.se
Phone: +46739737968

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JKDJH141CJ0XRN573B8GX8SB

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

NeoNavia base unit17350081940031
NeoNavia driver17350081940048