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Ascensia Diabetes Care Holdings AG

Switzerland CH-MF-000034124 Last updated 23 Oct 2026

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Devices
46
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue46

EUDAMED certificates16

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (16)

Notified body 2797 16 certificates

  • IVDR 785590 Issued

    Technical documentation EU IVDR

    Issued
    8 Jul 2025
    Expires
    7 Jul 2030
  • IVDR 785591 Issued

    Technical documentation EU IVDR

    Issued
    8 Jul 2025
    Expires
    7 Jul 2030
  • IVDR 785594 Issued

    Technical documentation EU IVDR

    Issued
    21 Oct 2024
    Expires
    20 Oct 2029
  • IVDR 785593 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    2 Sep 2029
    Reason
    Change approved
  • IVDR 785596 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    2 Sep 2029
    Reason
    Change approved
  • IVDR 785597 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    2 Sep 2029
    Reason
    Change approved
  • IVDR 785588 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    29 Aug 2029
    Reason
    Change approved
  • IVDR 785592 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    28 Aug 2029
    Reason
    Change approved
  • IVDR 785595 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    28 Aug 2029
    Reason
    Change approved
  • IVDR 789361 Issued

    Technical documentation EU IVDR

    Issued
    29 Aug 2024
    Expires
    28 Aug 2029
  • IVDR 745585 Amended

    Technical documentation EU IVDR

    Issued
    17 Nov 2025
    Expires
    15 Jun 2028
    Reason
    Other
  • IVDR 745588 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    15 Jun 2028
    Reason
    Change approved
  • IVDR 745590 Issued

    Technical documentation EU IVDR

    Issued
    16 Jun 2023
    Expires
    15 Jun 2028
  • IVDR 745593 Amended

    Technical documentation EU IVDR

    Issued
    17 Nov 2025
    Expires
    15 Jun 2028
    Reason
    Other
  • IVDR 745603 Supplemented

    Technical documentation EU IVDR

    Issued
    24 Aug 2026
    Expires
    15 Jun 2028
    Reason
    Change approved
  • IVDR 745580 Supplemented

    Quality management system EU IVDR

    Issued
    8 Jul 2025
    Expires
    16 May 2027
    Reason
    Add device or group

Related companies

Authorised representatives

Notified bodies

  • Notified body 2797

About

Ascensia Diabetes Care is a global company entirely dedicated to improving the health and lives of people with diabetes.

From the manufacturer's own website. Source

What Ascensia Diabetes Care Holdings AG makes

Ascensia Diabetes Care Holdings AG manufactures lancing devices, specifically the Microlet and Microlet Next product lines used for blood glucose monitoring.

These devices are classified as Class IIa medical devices and are listed in the EUDAMED database. The company is based in Switzerland.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What products does Ascensia Diabetes Care Holdings AG manufacture?

Ascensia Diabetes Care Holdings AG specializes in the production of lancing devices. Specifically, the company manufactures the Microlet and Microlet Next product lines, which are designed to be used for blood glucose monitoring purposes.

Where is Ascensia Diabetes Care Holdings AG based?

The company is based in Switzerland. This location is identified by the country code CH, which denotes the Swiss Confederation, where the company maintains its corporate operations.

How are the company's devices classified and where can I find them listed?

The lancing devices produced by the company are classified as Class IIa medical devices. These specific products are listed in the EUDAMED database, which serves as the central repository for information regarding medical devices within the European regulatory framework.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Switzerland
Address
90, Peter Merian Strasse, Basel, Switzerland
Phone
+41615608700
PRRC contact
Larnie James
EUDAMED SRN
CH-MF-000034124
FDA FEI number
3012118659