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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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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

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UDI-DI variants

312 UDI-DI variants

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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

AG03-085303700535122129
AG05-137203700535143001
ANC0621303700535164969
ANC0611003700535165287
ANC0651103700535165621
ANC0600303700535165256
ANC0601903700535164808
AG03-087603700535122242
ANC0652903700535165805
ANC0679403700535165973
AG02-060503700535119563
AG03-087203700535122204
ANC0679003700535165935
AG02-211203700535137062
ANC0603103700535164884
ANC06365103700535163993
AG02-201103700535120071
AG02-211303700535137079
ANC06364203700535163863
AG05-135203700535142905
ANC0651703700535165683
ANC06143403700535163740
ANC0622903700535165065
AG05-132403700535142769
AG02-401303700535156810

3 4 5 6 7

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