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.

Trial instruments -Knee — 312 UDI-DI variants, MDR

MD Atlas
X.NOV MEDICAL TECHNOLOGY

Data from EUDAMED, last updated May 31, 2026

Trial instruments -Knee

3700535100054Q4

312 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: X.NOV MEDICAL TECHNOLOGY

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

Reusable

Identity & classification

Basic UDI-DI: 3700535100054Q4
Device name: —
Device model: Trial instruments -Knee
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: X.NOV MEDICAL TECHNOLOGY
SRN: CH-MF-000018319
Country: Switzerland
Email: contact@xnov.com
Phone: +41 32 544 65 66

Authorised representative

Name: X.NOV
SRN: FR-AR-000007682
Country: France
Phone: +33 84 21 29 04

Variants by status

UDI-DI variants

312 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

basicUdiUlid01KSN08PSS6SEDVC6JHMA8X230

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

AG03-087503700535122235
AG05-121103700535142608
ANC0603403700535164891
ANC0636581103700535163597
ANC0636571103700535163559
AG02-201303700535120095
ANC0679103700535165942
ANC0621803700535164990
AG02-060303700535119549
ANC0613603700535165218
AG05-137003700535142981
ANC0601803700535164792
ANC0612803700535165133
ANC0626203700535165492
ANC061424903700535163429
ANC06364603700535163900
AG02-211403700535137086
ANC0652003700535165713
AG05-121403700535142639
AG05-120103700535142516
ANC0614251303700535163481
ANC0650503700535165560
AG03-085503700535122143
AG05-137103700535142998
ANC0650603700535165577

4 5 6 7 8