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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 Implants -Hip — 261 UDI-DI variants, MDR

MD Atlas
X.NOV MEDICAL TECHNOLOGY

Data from EUDAMED, last updated May 31, 2026

Trial Implants -Hip

3700535100015PS

261 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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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3700535100015PS
Device name: —
Device model: Trial Implants -Hip
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

261 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSNF2EE1ZRPSCPQ1B185JSAF

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

ANC0637603700535169827
ANC06107903700535169582
ANC06111903700535169506
ANC06108903700535169896
ANC0631203700535170229
ANC02169103700535169414
AH21-036203700535167717
ANC06202303700535170151
AH11-100303700535126615
AH06-116403700535162965
AH11-140303700535126813