Skip to content

Siemens Healthcare Diagnostics Inc.

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000016560 FEI 2432235

Devices
2,137
Registrations
EUDAMEDFDA
FDA recalls
0

Catalogue2,137

Newest first, rows 51-100 of 2,137

Search and filter all 2,137 devices
Skip device list

Rows 51-100 of 2,137

Showing 51-100 of 2,137

Company details

EUDAMED SRN
US-MF-000016560
FDA FEI number
2432235
DUNS number
005088112
EUDAMED status
Active
EUDAMED registered name
Siemens Healthcare Diagnostics Inc.
Registered address
511, Benedict Avenue, NY 10591, Tarrytown, United States
Phone
+1 877 229 3711
PRRC contact
Robert Brennan(public in EUDAMED)
1 more person
  • Erin Hansen

EUDAMED certificates22

22 certificates20 valid, 2 expiredIVDR 22next expiry 3 Mar 2027

EUDAMED certificates (22)

TÜV Rheinland LGA Products GmbH 0197 22 certificates

  • IX 1290554-35 Active

    Technical documentation EU IVDR

    Issued
    18 Jul 2025
    Expires
    17 Jul 2030
  • IX 1290554-36 Active

    Technical documentation EU IVDR

    Issued
    14 Jul 2025
    Expires
    13 Jul 2030
  • IX 1290554-11 Active

    Technical documentation EU IVDR

    Issued
    9 Dec 2024
    Expires
    8 Dec 2029
  • IX 1290554-14 Active

    Technical documentation EU IVDR

    Issued
    9 Dec 2024
    Expires
    8 Dec 2029
  • IX 1290554-30 Active

    Technical documentation EU IVDR

    Issued
    12 Mar 2024
    Expires
    11 Mar 2029
  • IX 1290554-31 Active

    Technical documentation EU IVDR

    Issued
    7 Mar 2024
    Expires
    6 Mar 2029
  • IX 1290554-12 Active

    Technical documentation EU IVDR

    Issued
    2 Feb 2024
    Expires
    1 Feb 2029
  • IX 1290554-23 Active

    Technical documentation EU IVDR

    Issued
    1 Sep 2023
    Expires
    31 Aug 2028
  • IX 1290554-25 Active Supplemented

    Technical documentation EU IVDR

    Issued
    17 Jul 2024
    Expires
    1 Aug 2028
    Reason
    Add device or group
  • IX 1290554-28 Active

    Technical documentation EU IVDR

    Issued
    3 Jul 2024
    Expires
    1 Aug 2028
  • IX 1290554-1 Active

    Technical documentation EU IVDR

    Issued
    3 Jul 2023
    Expires
    2 Jul 2028
  • IX 1290554-16 Active

    Technical documentation EU IVDR

    Issued
    3 Jul 2023
    Expires
    2 Jul 2028
  • IX 1290554-10 Active

    Technical documentation EU IVDR

    Issued
    27 Nov 2025
    Expires
    25 Jun 2028
  • IX 1290554-7 Active

    Technical documentation EU IVDR

    Issued
    12 May 2025
    Expires
    5 Jun 2028
  • IX 1290554-8 Active Amended

    Technical documentation EU IVDR

    Issued
    12 May 2025
    Expires
    5 Jun 2028
    Reason
    Other
  • IX 1290554-20 Active

    Technical documentation EU IVDR

    Issued
    6 Sep 2024
    Expires
    6 Mar 2028
  • IX 1290554-17 Expiring Expires in 328 days

    Technical documentation EU IVDR

    Issued
    2 Nov 2022
    Expires
    26 Sep 2027
  • IX 1290554-18 Expiring Expires in 288 days

    Technical documentation EU IVDR

    Issued
    18 Aug 2022
    Expires
    17 Aug 2027
  • HX 7091841-1 Restricted

    Quality management system EU IVDR

    Issued
    26 Aug 2026
    Expires
    7 Mar 2027
    Reason
    Not on market
  • HX 1290554-1 Expiring Supplemented Expires in 121 days

    Quality management system EU IVDR

    Issued
    5 Oct 2026
    Expires
    3 Mar 2027
    Reason
    Add device or group
  • HX 7091841-1 Expired

    Quality management system EU IVDR

    Issued
    6 Feb 2026
    Expires
    26 Oct 2026
    Reason
    Add device or group
  • HX 1290554-1 Expired

    Quality management system EU IVDR

    Issued
    29 Mar 2026
    Expires
    15 Sep 2026
    Reason
    Add device or group

From the company website

Read 18 Oct 2026

We pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Discover more about our innovative medtech and the people behind it.

From the manufacturer's own website. Source