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.

NeuroLF — 3 UDI-DI variants, MDR (Positrigo AG)

MD Atlas
Positrigo AG

Data from EUDAMED, last updated May 23, 2026

NeuroLF

7649998522NeuroLFME

3 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: Positrigo AG

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

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 7649998522NeuroLFME
Device name: NeuroLF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Positrigo AG
SRN: CH-MF-000018932
Country: Switzerland
Email: info@positrigo.com

Authorised representative

Name: Positrigo Germany GmbH
SRN: DE-AR-000017987
Country: Germany

Variants by status

UDI-DI variants

3 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

basicUdiUlid01GG7KB6W6WZ7XJF06ZVBZZWDY

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

NLF-1000-00007649998522038
NLF-1000-200007649998522014
NLF-1000-100007649998522021