Waldemar Link GmbH & Co. KG
Germany DE-MF-000005215 Last updated 25 Oct 2026
- Devices
- 1,228
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
C.F.P. Hip Stem Ref 290-163/17
GEMINI SL Total Knee System Ref 318-812/18
Cemented Acetabular Cup System Ref 105-415/60
SPII Model Lubinus Hip Stem Ref 127-963/26
LCU Hip System Ref 165-518/26
SPII Model Lubinus Hip Stem Ref 99-0017/29
Cemented Acetabular Cup System Ref 105-415/56
SPII Model Lubinus Hip Stem Ref 99-0005/77
SPII Model Lubinus Hip Stem Ref 127-956/35
LINK Embrace Shoulder System Ref 643-136/03
LINK Embrace Shoulder System Ref 642-150/16
GEMINI SL Total Knee System Ref 318-444/12
Endo-Model Knee System / LINK Endo-Model EVO Knee System Ref 15-8551/36
LINK Embrace Shoulder System Ref 647-147/17
Pelvis Support Type RR and Type RC Ref 15-8350/62
GEMINI SL Total Knee System Ref 318-212/25
Cemented Acetabular Cup System Ref 105-400/54
TrabecuLink Augments and Bone Screws Ref 64-7710/10
Vario-Cup System Ref 99-0055/51
LINK Embrace Shoulder System Ref 645-057/64
LINK Embrace Shoulder System Ref 640-010/40
GEMINI SL Total Knee System Ref 318-212/26
LinkSymphoKnee Ref 880-130/30
LINK Embrace Shoulder System Ref 647-144/16
Cemented Acetabular Cup System Ref 110-018/56
SPII Model Lubinus Hip Stem Ref 127-956/26
SPII Model Lubinus Hip Stem Ref 99-2728/17
Cemented Acetabular Cup System Ref 102-130
TrabecuLink Augments and Bone Screws Ref 64-9081/56
SPII Model Lubinus Hip Stem Ref 99-2724/26
Endo-Model Knee System / LINK Endo-Model EVO Knee System Ref 15-0027/42
SPII Model Lubinus Hip Stem Ref 127-945/26
LINK Embrace Shoulder System Ref 643-142/16
C.F.P. Hip Stem Ref 290-179/26
Cemented Acetabular Cup System Ref 120-275
GEMINI SL Total Knee System Ref 318-438/12
SPII Model Lubinus Hip Stem Ref 127-959/26
C.F.P. Hip Stem Ref 290-175/26
Cemented Acetabular Cup System Ref 110-020/56
C.F.P. Hip Stem Ref 290-162/26
LINK Embrace Shoulder System Ref 643-642/13
LinkSymphoKnee Ref 880-130/X0
Cemented Acetabular Cup System Ref 105-410/62
GEMINI SL Total Knee System Ref 318-376/03
LinkSymphoKnee Ref 880-120/35
GEMINI SL Total Knee System Ref 318-216/26
LINK Embrace Shoulder System Ref 643-642/03
MP Reconstruction System Ref 137-045/38
GEMINI SL Total Knee System Ref 318-313/01
LinkSymphoKnee Ref 880-111/00
Showing 1-50 of 1,228
EUDAMED certificates
Notified body 0482 24 certificates
- 20637GB450260728 Issued
Technical documentation EU MDR
- Issued
- 28 Jul 2026
- Expires
- 27 Jul 2031
- 20625GB450260722 Issued
Technical documentation EU MDR
- Issued
- 22 Jul 2026
- Expires
- 21 Jul 2031
- 20623GB450260709 Issued
Technical documentation EU MDR
- Issued
- 9 Jul 2026
- Expires
- 8 Jul 2031
- 20213GB450260528 Reissued
Technical documentation EU MDR
- Issued
- 28 May 2026
- Expires
- 6 Jun 2031
- Valid from
- 7 Jun 2026
- 20624GB450260507 Issued
Technical documentation EU MDR
- Issued
- 7 May 2026
- Expires
- 6 May 2031
- 20619GB450260504 Issued
Technical documentation EU MDR
- Issued
- 4 May 2026
- Expires
- 3 May 2031
- 20609GB450251216 Issued
Technical documentation EU MDR
- Issued
- 16 Dec 2025
- Expires
- 15 Dec 2030
- 13787GB450250227 Issued
Technical documentation EU MDR
- Issued
- 27 Feb 2025
- Expires
- 26 Feb 2030
- 13697GB450250204 Issued
Technical documentation EU MDR
- Issued
- 4 Feb 2025
- Expires
- 3 Feb 2030
- 13806GB450241217 Issued
Technical documentation EU MDR
- Issued
- 17 Dec 2024
- Expires
- 16 Dec 2029
- 13792GB450240723 Issued
Technical documentation EU MDR
- Issued
- 23 Jul 2024
- Expires
- 22 Jul 2029
- 13791GB450260302 Supplemented
Technical documentation EU MDR
- Issued
- 2 Mar 2026
- Expires
- 10 Jul 2029
- Reason
- Add device or group
- 13794GB450240710 Issued
Technical documentation EU MDR
- Issued
- 10 Jul 2024
- Expires
- 9 Jul 2029
- 13780GB450240709 Issued
Technical documentation EU MDR
- Issued
- 9 Jul 2024
- Expires
- 8 Jul 2029
- 13785GB450240524 Issued
Technical documentation EU MDR
- Issued
- 24 May 2024
- Expires
- 23 May 2029
- 13789GB450240524 Issued
Technical documentation EU MDR
- Issued
- 24 May 2024
- Expires
- 23 May 2029
- 13786GB450260609 Supplemented
Technical documentation EU MDR
- Issued
- 9 Jun 2026
- Expires
- 16 May 2029
- Reason
- Change approved
- 20399GB450240517 Issued
Technical documentation EU MDR
- Issued
- 17 May 2024
- Expires
- 16 May 2029
- 13783GB450240125 Issued
Technical documentation EU MDR
- Issued
- 25 Jan 2024
- Expires
- 24 Jan 2029
- 13803GB450251029 Supplemented
Technical documentation EU MDR
- Issued
- 29 Oct 2025
- Expires
- 17 Jan 2029
- Reason
- Add device or group
- 13804GB450250207 Supplemented
Technical documentation EU MDR
- Issued
- 7 Feb 2025
- Expires
- 28 Sep 2028
- Reason
- Add device or group
- 13691GB450220701 Issued
Technical documentation EU MDR
- Issued
- 1 Jul 2022
- Expires
- 30 Jun 2027
- 13690GB450220711 Amended
Technical documentation EU MDR
- Issued
- 11 Jul 2022
- Expires
- 9 Jun 2027
- Reason
- Other
- 20271GB450220502 Issued
Technical documentation EU MDR
- Issued
- 2 May 2022
- Expires
- 1 May 2027
ITALCERT SRL 0426 1 certificate
- 057-00-02-MDR Supplemented
Technical documentation EU MDR
- Issued
- 13 May 2025
- Expires
- 12 Sep 2029
- Reason
- Other
Related companies
Notified bodies
- Notified body 0482
- ITALCERT SRL 0426
About
For all of us, retaining our mobility is essential. In many ways, it is key to leading an independent, active life. That’s why we at LINK are driven by the goal of enabling people who need a joint prosthesis to live a normal life, free of pain. As an owner-managed firm, based in the city of Hamburg, we set standards in primary and revision arthroplasty of major joints. Our extensive product range means that we are able to offer the optimal solution for each specific case and personal requirements – with high-quality, innovative and bioharmonious prostheses.
What Waldemar Link GmbH & Co. KG makes
Waldemar Link GmbH & Co. KG manufactures cemented acetabular cup systems and cementless C.F.P. hip stems for primary and revision arthroplasty of the hip joint. These products are designed to restore mobility and function in patients requiring joint replacement surgery.
The company’s devices are classified as Class III medical devices and are registered in the EU via the eudamed database. The manufacturer is based in Germany.
Frequently asked questions
What types of medical devices does Waldemar Link GmbH & Co. KG manufacture?
Waldemar Link GmbH & Co. KG specializes in orthopedic implants for hip joint replacement. Specifically, they produce cemented acetabular cup systems and cementless C.F.P. hip stems, which are designed for both primary and revision arthroplasty procedures. These devices are intended to restore mobility and function in patients who require joint replacement surgery.
Where is Waldemar Link GmbH & Co. KG based?
The company is headquartered in Hamburg, Germany. Being based in Germany aligns with its focus on high-quality, innovative medical devices tailored for joint replacement surgeries, reflecting its commitment to precision and patient care.
Which regulatory registries list Waldemar Link GmbH & Co. KG’s devices?
Waldemar Link GmbH & Co. KG’s devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices authorized for use within the EU.
How are Waldemar Link GmbH & Co. KG’s devices classified under EU regulations?
The company’s devices are classified as Class III medical devices under EU regulations. This classification applies to products that support or sustain life, are of significant risk, or present a potential unreasonable risk of illness or injury. Hip joint replacements fall under this category due to their critical role in restoring mobility and function.
Information
- Country
- Germany
- Address
- 10, Barkhausenweg, Hamburg, Germany
- Website
- www.linkorthopaedics.com
- [email protected]
- Phone
- +49 40 53995 0
- PRRC contact
- Poroshat Khalilpour
- EUDAMED SRN
- DE-MF-000005215
- FDA FEI number
- 3003386935