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Neuromedex GmbH

Germany DE-MF-000005867 Last updated 25 Oct 2026

Devices
37
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue37

EUDAMED certificates3

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

EUDAMED certificates (3)

Notified body 0482 3 certificates

  • 10555GB450260803 Issued

    Technical documentation EU MDR

    Issued
    3 Aug 2026
    Expires
    2 Aug 2031
  • 10551GB450260311 Reissued

    Technical documentation EU MDR

    Issued
    11 Mar 2026
    Expires
    5 Jan 2028
  • 1261GB448260326 Supplemented

    Quality management system EU MDR

    Issued
    26 Mar 2026
    Expires
    12 Apr 2027
    Reason
    Add device or group

Notified bodies

  • Notified body 0482

What Neuromedex GmbH makes

Neuromedex GmbH manufactures Mediloops® Gefäßschlinge (vascular loops) and Temporäre Myokardiale Elektrode (TME), which are temporary myocardial electrodes.

These devices are classified as Class I, Class IIa, Class IIb, and Class III and are listed in the EUDAMED registry; the company is based in Germany.

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

Frequently asked questions

What does Neuromedex GmbH manufacture?

Neuromedex GmbH manufactures Mediloops® Gefäßschlinge (vascular loops) and Temporäre Myokardiale Elektrode (TME), which are temporary myocardial electrodes, as stated in the provided device data summary.

Where is Neuromedex GmbH based?

Neuromedex GmbH is based in Germany, as indicated by the country code DE in the device data and confirmed in the summary stating the company is based in Germany.

In which registry are Neuromedex GmbH's devices listed?

Neuromedex GmbH's devices are listed in the EUDAMED registry, as explicitly stated in the LISTED IN field and reiterated in the summary.

How are Neuromedex GmbH's devices classified?

Neuromedex GmbH's devices are classified as Class I, Class IIa, Class IIb, and Class III, as specified in the DEVICE CLASSES field and confirmed in the summary.

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

Information

Country
Germany
Address
15, Vierenkamp, Hamburg, Germany
Phone
+49 40 696 564 0
PRRC contact
Victor Huvale
EUDAMED SRN
DE-MF-000005867
FDA FEI number
3009829742