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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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TrabecuLink Femoral and Tibial Cones — 2 UDI-DI variants, MDR

MD Atlas
Waldemar Link GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

TrabecuLink Femoral and Tibial Cones

4026575-1-KNR-252007-YR

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Waldemar Link GmbH & Co. KG

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Device characteristics

Implantable

Legacy certificates

Certificate number: 20609GB450251216
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: DNV MEDCERT GmbH (0482)
Validity: Dec 16, 2025 → Dec 15, 2030

Identity & classification

Basic UDI-DI: 4026575-1-KNR-252007-YR
Device name: TrabecuLink Femoral and Tibial Cones
Device model: Femoral cone, uncemented, Ti6Al4V - 3D-printed, proximal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Waldemar Link GmbH & Co. KG
SRN: DE-MF-000005215
Country: Germany
Email: info@linkhh.de
Phone: +49 40 53995 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KP373ZN0HXTV10Z203AGGRER

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

15-3992/0704026575182435
15-3994/0704026575182473