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Waldemar Link GmbH & Co. KG

Active in EUDAMED

Germanyfrom SRN EUDAMED FDA SRN DE-MF-000005215 FEI 3003386935

Devices
1,228
Registrations
EUDAMEDFDA
FDA recalls
0

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.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1,228

Newest first, rows 101-150 of 1,228

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  • GEMINI SL Total Knee System Ref 318-453/05

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • SPII Model Lubinus Hip Stem Ref 127-961/35

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • LINK Embrace Shoulder System Ref 643-539/03

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • TrabecuLink Augments and Bone Screws Ref 109-322/50

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • Cemented Acetabular Cup System Ref 102-116

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • TrabecuLink Augments and Bone Screws Ref 64-9074/42

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • Cemented Acetabular Cup System Ref 102-110

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • SPII Model Lubinus Hip Stem Ref 99-2766/26

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 104-105

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • SPII Model Lubinus Hip Stem Ref 99-2762/17

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-811/16

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 110-120/66

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 102-134

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 105-415/50

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • LinkSymphoKnee Ref 880-110/45

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-432/14

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • SPII Model Lubinus Hip Stem Ref 127-738/17

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • SPII Model Lubinus Hip Stem Ref 127-772/17

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 101-112

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 110-020/52

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • LinkSymphoKnee Ref 880-120/90

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-213/16

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-811/12

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-216/25

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-434/16

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • TrabecuLink Augments and Bone Screws Ref 64-9066/26

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • TrabecuLink Augments and Bone Screws Ref 64-9082/58

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • GEMINI SL Total Knee System Ref 318-453/01

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Pelvis Support Type RR and Type RC Ref 15-8330/50

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • GEMINI SL Total Knee System Ref 318-811/18

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 15-1019/54

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-213/25

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • MP Reconstruction System Ref 137-065/38

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Pelvis Support Type RR and Type RC Ref 15-8330/56

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • SPII Model Lubinus Hip Stem Ref 99-2768/17

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 110-118/56

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Cemented Acetabular Cup System Ref 110-012/38

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-802/14

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • MobileLink Acetabular Cup System Ref 183-550/36

    Expiring Regimes: CE MDR Registry: EUDAMED Class:III

  • LCU Hip System Ref 165-621/26

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Pelvis Support Type RR and Type RC Ref 15-8300/46

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • LINK Embrace Shoulder System Ref 645-041/52

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • GEMINI SL Total Knee System Ref 318-337/04

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Pelvis Support Type RR and Type RC Ref 15-8310/52

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • TrabecuLink Augments and Bone Screws Ref 64-9098/97

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • Cemented Acetabular Cup System Ref 15-1010/44

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • TrabecuLink Augments and Bone Screws Ref 64-9067/28

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • SPII Model Lubinus Hip Stem Ref 99-0005/79

    Active Regimes: CE MDR Registry: EUDAMED Class:III

  • Pelvis Support Type RR and Type RC Ref 15-8310/54

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb

  • Cemented Acetabular Cup System Ref 110-018/64

    Active Regimes: CE MDR Registry: EUDAMED Class:III

Rows 101-150 of 1,228

Showing 101-150 of 1,228

Company details

EUDAMED SRN
DE-MF-000005215
FDA FEI number
3003386935
EU VAT number
DE118451256
EUDAMED status
Active
EUDAMED registered name
Waldemar Link GmbH & Co. KG
EUDAMED abbreviated name
LINK
Registered address
10, Barkhausenweg, 22339, Hamburg, Germany
Phone
+49 40 53995 0
PRRC contact
Poroshat Khalilpour(public in EUDAMED)

EUDAMED certificates26

26 certificates26 valid, 0 expiredMDR 26next expiry 1 May 2027

EUDAMED certificates (26)

DNV MEDCERT GmbH 0482 25 certificates

  • 20637GB450260728 Active

    Technical documentation EU MDR

    Issued
    28 Jul 2026
    Expires
    27 Jul 2031
  • 20625GB450260722 Active

    Technical documentation EU MDR

    Issued
    22 Jul 2026
    Expires
    21 Jul 2031
  • 20623GB450260709 Active

    Technical documentation EU MDR

    Issued
    9 Jul 2026
    Expires
    8 Jul 2031
  • 20213GB450260528 Active Reissued

    Technical documentation EU MDR

    Issued
    28 May 2026
    Expires
    6 Jun 2031
    Valid from
    7 Jun 2026
  • 20624GB450260507 Active

    Technical documentation EU MDR

    Issued
    7 May 2026
    Expires
    6 May 2031
  • 20619GB450260504 Active

    Technical documentation EU MDR

    Issued
    4 May 2026
    Expires
    3 May 2031
  • 20609GB450251216 Active

    Technical documentation EU MDR

    Issued
    16 Dec 2025
    Expires
    15 Dec 2030
  • 7402GB448261021 Active Supplemented

    Quality management system EU MDR

    Issued
    21 Oct 2026
    Expires
    30 Sep 2030
    Reason
    Change approved
  • 13787GB450250227 Active

    Technical documentation EU MDR

    Issued
    27 Feb 2025
    Expires
    26 Feb 2030
  • 13697GB450250204 Active

    Technical documentation EU MDR

    Issued
    4 Feb 2025
    Expires
    3 Feb 2030
  • 13806GB450241217 Active

    Technical documentation EU MDR

    Issued
    17 Dec 2024
    Expires
    16 Dec 2029
  • 13792GB450240723 Active

    Technical documentation EU MDR

    Issued
    23 Jul 2024
    Expires
    22 Jul 2029
  • 13791GB450260302 Active Supplemented

    Technical documentation EU MDR

    Issued
    2 Mar 2026
    Expires
    10 Jul 2029
    Reason
    Add device or group
  • 13794GB450240710 Active

    Technical documentation EU MDR

    Issued
    10 Jul 2024
    Expires
    9 Jul 2029
  • 13780GB450240709 Active

    Technical documentation EU MDR

    Issued
    9 Jul 2024
    Expires
    8 Jul 2029
  • 13785GB450240524 Active

    Technical documentation EU MDR

    Issued
    24 May 2024
    Expires
    23 May 2029
  • 13789GB450240524 Active

    Technical documentation EU MDR

    Issued
    24 May 2024
    Expires
    23 May 2029
  • 13786GB450260609 Active Supplemented

    Technical documentation EU MDR

    Issued
    9 Jun 2026
    Expires
    16 May 2029
    Reason
    Change approved
  • 20399GB450240517 Active

    Technical documentation EU MDR

    Issued
    17 May 2024
    Expires
    16 May 2029
  • 13783GB450240125 Active

    Technical documentation EU MDR

    Issued
    25 Jan 2024
    Expires
    24 Jan 2029
  • 13803GB450251029 Active Supplemented

    Technical documentation EU MDR

    Issued
    29 Oct 2025
    Expires
    17 Jan 2029
    Reason
    Add device or group
  • 13804GB450250207 Active Supplemented

    Technical documentation EU MDR

    Issued
    7 Feb 2025
    Expires
    28 Sep 2028
    Reason
    Add device or group
  • 13691GB450220701 Expiring Expires in 241 days

    Technical documentation EU MDR

    Issued
    1 Jul 2022
    Expires
    30 Jun 2027
  • 13690GB450220711 Expiring Amended Expires in 220 days

    Technical documentation EU MDR

    Issued
    11 Jul 2022
    Expires
    9 Jun 2027
    Reason
    Other
  • 20271GB450220502 Expiring Expires in 181 days

    Technical documentation EU MDR

    Issued
    2 May 2022
    Expires
    1 May 2027

ITALCERT SRL 0426 1 certificate

  • 057-00-02-MDR Active Supplemented

    Technical documentation EU MDR

    Issued
    13 May 2025
    Expires
    12 Sep 2029
    Reason
    Other

From the company website

Read 18 Oct 2026

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.

From the manufacturer's own website. Source