Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

1085 ICS Impulse System — 13 UDI-DI variants, MDR

MD Atlas
Natus Medical Denmark ApS

Data from EUDAMED, last updated May 23, 2026

1085 ICS Impulse System

5713315NA001014X

13 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: Natus Medical Denmark ApS

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5713315NA001014X
Device name: 1085 ICS Impulse System
Device model: 1085 ICS Impulse System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Natus Medical Denmark ApS
SRN: DK-MF-000001617
Country: Denmark
Email: martha.kennedy@natus.com
Phone: +353-91-647433

Variants by status

UDI-DI variants

13 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KGM95SHCV91C14BYX9M3CD9T

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

1085 Face Cushion (10 Boxes/120 Cushions)05713315008498
1085 Face Cushion 2 (10 Boxes/100 Cushions)05713315005862
1085 ICS Impulse Incl. Lateral Head Impulse05713315007149
1085 ICS Impulse Mono. Ocu. Ltd., Lateral Head Imp, LARP/RALP Head Imp, Mono. Pos., Tors.05713315007163
1085 ICS Impulse Monocular Ocu. Ltd.,Lateral Head Imp,LARP/RALPHead Imp, Mono. Positional05713315007194
1085 ICS Impulse Monocular Video Frenzel Only05713315007170
1085 ICS Impulse, Incl. Lateral Head Impulse, LARP/RALP Head Impulse05713315007156
1085 ICS Impulse, Incl. Monocular Ocu. Ltd., Lateral Head Impulse, LARP/RALP Head Impulse05713315007187
1085 ICS Impulse, Mono. Ocu. Ltd., Lateral Head Impulse, LARP/RALP HeadImpulse, Torsional05713315007132
ICS Impulse (Full w/o webcam Hardware - Lateral/LARP/RALP/Synchrontized Room Video)05713315007125
ICS Impulse (Full w/webcam Hardware - Lateral/LARP/RALP/Synchrontized Room Video)05713315007118
ICS Impulse Lateral, LARP/RALP, DSral, LARP/RALP, DS05713315008009
vHIT ICS Impulse05713315008047