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.

TrabecuLink Femoral and Tibial Cones — 24 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-252005-YK

24 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

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

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-252005-YK
Device name: TrabecuLink Femoral and Tibial Cones
Device model: Femoral cone, uncemented, Ti6Al4V - 3D-printed, 3-zones
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

24 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

basicUdiUlid01KP35DE7F0M8ZZ7FAYECFNZWH

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

15-3995/0104026575265145
15-3994/0204026575265237
15-3998/0204026575265299
15-3996/0204026575265251
15-3992/0304026575265312
15-3997/0304026575265459
15-3998/0104026575265190
15-3998/0304026575265497
15-3997/0104026575265183
15-3992/0104026575265114
15-3992/0204026575265213
15-3991/0304026575265305
15-3991/0104026575265107
15-3994/0304026575265367
15-3996/0104026575265176
15-3997/0204026575265275
15-3995/0204026575265244
15-3996/0304026575265428
15-3993/0304026575265336
15-3994/0104026575265138
15-3991/0204026575265206
15-3993/0204026575265220
15-3995/0304026575265381
15-3993/0104026575265121