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

ANC0622503700535165041
ANC0612903700535165140
AG02-060103700535119525
ANC0652303700535165744
AG05-136603700535142974
AG03-124103700535122822
AG03-112503700535122600
AG05-132203700535142752
AG05-121503700535142646
AG05-120303700535142530
ANC0652503700535165768
AG05-135603700535142929