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TauroPharm GmbH

Germany DE-MF-000008314 Last updated 21 Oct 2026

Devices
29
Registries
EUDAMED
FDA recalls
0

Catalogue29

EUDAMED certificates3

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

EUDAMED certificates (3)

TÜV SÜD Product Service GmbH 0123 3 certificates

  • G70 051963 0029 Issued

    Technical documentation EU MDR

    Issued
    21 Apr 2023
    Expires
    20 Apr 2028
  • G70 051963 0027 Supplemented

    Technical documentation EU MDR

    Issued
    25 Jun 2026
    Expires
    15 Aug 2027
    Reason
    Add device or group
  • G12 051963 0028 Issued

    Quality management system EU MDR

    Issued
    20 Jul 2022
    Expires
    19 Jul 2027

Notified bodies

About

We develop antimicrobial solutions for central-venous catheters & cardiac pacemakers to protect patients against complications.

From the manufacturer's own website. Source

What TauroPharm GmbH makes

TauroPharm GmbH manufactures sterile medical sets designed for intravenous therapy, including hanging sets for central venous catheters (ZVK) and port systems, as well as completion sets for intravenous nutrition therapy and total parenteral nutrition (TPN). Their products include variations with added saline (NaCl) for flushing or priming, such as the APOSAN and WB Simple & Safe sets, which are tailored for specific clinical applications like catheter lock solutions and infusion therapy.

The company’s devices are classified under EU regulations as Class IIa, Class IIb, and Class III, reflecting varying levels of risk and regulatory scrutiny. These products are registered in the EU’s eudamed database, adhering to European Medical Device Regulation (MDR) requirements. TauroPharm GmbH 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 types of medical devices does TauroPharm GmbH manufacture?

TauroPharm GmbH specializes in sterile medical sets primarily used for intravenous therapy. Their products include hanging sets for central venous catheters (ZVK) and port systems, as well as completion sets for intravenous nutrition therapy and total parenteral nutrition (TPN). Many of these sets incorporate added saline (NaCl) for flushing or priming purposes, such as the APOSAN and WB Simple & Safe lines, which are designed for specific clinical applications like catheter lock solutions and infusion therapy.

Where is TauroPharm GmbH based?

TauroPharm GmbH is headquartered in Germany. The company’s location in Germany aligns with European regulatory frameworks, ensuring compliance with EU medical device standards and requirements.

Which regulatory registries list TauroPharm GmbH’s devices?

TauroPharm GmbH’s devices are registered in the eudamed database, which is the official EU portal for medical device information under the European Medical Device Regulation (MDR). This registry ensures transparency and traceability of devices authorized for use within the European Economic Area.

How are TauroPharm GmbH’s devices classified under EU regulations?

TauroPharm GmbH’s devices fall into Class IIa, Class IIb, and Class III classifications under EU medical device regulations. These classifications are determined by risk levels: Class III devices pose the highest risk (e.g., those directly supporting life or involving long-term implantation), while Class IIa and IIb devices carry moderate or lower risks. The classification influences the regulatory scrutiny and documentation requirements for each product.

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

Information

Country
Germany
Address
51, August-Bebel-Str., Waldbüttelbrunn, Germany
Phone
+499313942990(from company website)
EUDAMED SRN
DE-MF-000008314