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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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Lumbar Instruments — 184 UDI-DI variants, MDR (NGMedical GmbH)

MD Atlas
NGMedical GmbH

Data from EUDAMED, last updated May 23, 2026

Lumbar Instruments

42516314TD012I49

184 UDI-DI variants

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

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

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42516314TD012I49
Device name: Lumbar Instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: NGMedical GmbH
SRN: DE-MF-000000204
Country: Germany
Email: info@ngmedical.de
Phone: +49 6873999970

Variants by status

UDI-DI variants

184 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K88E90SABSECR50H3GZB46CN

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

T-Handle04251631416142
T-Handle04251631411291
T-Handle04251631410843
T-Handle long04251631416159
T-Handle long04251631410850
T-Handle long04251631411307
Torque Handle 10Nm04251631405481
Wrench / Retractor04251631408697
Wrench / Retractor04251631415879

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