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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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Knee instrumentation — 134 UDI-DI variants, MDR

MD Atlas
X.NOV MEDICAL TECHNOLOGY

Data from EUDAMED, last updated May 31, 2026

Knee instrumentation

3700535100014PQ

134 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: X.NOV MEDICAL TECHNOLOGY

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3700535100014PQ
Device name: —
Device model: Knee instrumentation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

134 UDI-DI variants

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Applied filters

basicUdiUlid01KSNF27XVN7RN7WQA0S6RSCQ4

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

No registered UDI-DI variants for this device family.