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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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NS96 Disc Remover — 2 UDI-DI variants, IVDR

MD Atlas
Labsystems Diagnostics Oy

Data from EUDAMED, last updated May 23, 2026

NS96 Disc Remover

6438172555I0001TR

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Labsystems Diagnostics Oy

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 6438172555I0001TR
Device name: NS96 Disc Remover
Device model: 5550300
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: Labsystems Diagnostics Oy
SRN: FI-MF-000018281
Country: Finland
Email: registrations@labsystemsdx.com
Phone: +358 20 155 7530

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9BFV60YZ1W9V0ZAYGM3VHJG

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

555040006438172555013
555030006438172555020