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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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Cervical Instruments — 37 UDI-DI variants, MDR (NGMedical GmbH)

MD Atlas
NGMedical GmbH

Data from EUDAMED, last updated May 23, 2026

Cervical Instruments

42516314TD020Ir4C

37 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: 42516314TD020Ir4C
Device name: Cervical 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

37 UDI-DI variants

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Applied filters

basicUdiUlid01K88G1NGEZ2S14KABNZ3RZDZE

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

Hammer 110g04251631400196
Intradical Spreader04251631416128
MOVE-C Distraction Rod04251631400301
MOVE-C Distraction Rod04251631412557
MOVE-C Distraction Rod04251631415862
MOVE-C Impactor04251631400318
MOVE-C Impactor04251631412588
MOVE-C Reposition Forceps04251631400103
MOVE-C Reposition Forceps04251631416081
MOVE-C Reposition Forceps04251631412571
Slide Hammer 200g04251631400110
Slide Hammer 200g04251631411123

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