TauroPharm GmbH
Germany DE-MF-000008314 Last updated 21 Oct 2026
- Devices
- 29
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Set 13S Abhängeset für ZVK und Portsysteme Ref 121113S
APOSAN Set B Ref 100154
WB Simple & Safe - Set 3b Ref 121WB3B
WB Simple & Safe - Set 2a Ref 121WB2A
WB Simple & Safe - Set 2a Ref 121WB2B
Set 11 (mit 3 x 10 ml NaCI) für ZVK und Portsysteme Ref 1211511S
WB Simple & Safe - Set 3a Ref 121WB3A
TauroLock™-U25.000 Ref TP-05
TauroLock™-HEP100 Ref TP-03-3
WB Simple & Safe - Set 1a Ref 121WB1A
TauroGuard™ 250ml Ref TP-09-250
TauroLock™ Ref TP-01-5
TauroGuard™ 100ml Ref TP-09-100
TP SalineFlush™ Ref TP-50-10
NutriLock™ Ref TP-07-3
TauroLock™ Ref TP-01-3
TauroPace™ Ref TP-08-250
EUDAMED certificates
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
Related companies
Notified bodies
About
We develop antimicrobial solutions for central-venous catheters & cardiac pacemakers to protect patients against complications.
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.
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.
Information
- Country
- Germany
- Address
- 51, August-Bebel-Str., Waldbüttelbrunn, Germany
- Website
- www.tauropharm.com
- [email protected]
- Phone
- +499313942990
- EUDAMED SRN
- DE-MF-000008314