PROMECON GmbH
Germany DE-MF-000015290 Last updated 21 Oct 2026
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- Devices
- 30
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SonoGuard Plus Set Ref SG.20.180.040-G
OptiGuard QuickChange Plus Ref OG.41.140.250
SonoGuard Plus Ref SG.20.180.160
CareVis Set Ref CS.20.VX214T.150
OptiGuard QuickChange Ref OG.40.180.250
SonoGuard Ref SG.10.140.080
SonoGuard Plus Set Ref SG.20.180.120-G
SonoGuard Plus Ref SG.20.180.120
CareVis Set Ref CS.00.VX214
SonoGuard Ref SG.10.140.120
Krystal Ref AC372
CareVis Set Ref CS.00.VX17
OptiGuard QuickChange Ref OG.40.140.250
SonoGuard Ref SG.10.140.040
OptiGuard Access Ref OG.10.130.250
OptiGuard QuickChange Plus Ref OG.41.180.250
CareVis Set Ref CS.10.M2060E.025
SonoGuard Plus Set Ref SG.20.180.080-G
SonoGuard Plus Ref SG.20.180.040
CareVis Set Ref CS.10.M2000.025
SonoGuard Ref SG.10.140.025
CareVis Set Ref CS.10.VM17.025
SonoGuard Plus Ref SG.20.180.080
SonoGuard Ref SG.10.140.160
CareVis Set Ref CS.20.VX214T.025
SonoGuard Plus Set Ref SG.20.180.160-G
CareVis Bag I/L Ref TT002
CareVis Bag S/M Ref TT001
CareVis Set Ref CS.10.VX214.065
CareVis Bag X/G Ref TT003
About
Herstellung und Vertrieb von Einmal-Medizinprodukten | ► Infusionspumpen ► Geräteabdeckungen ► HF-Instrumente ► Chirurgische Instrumente ► und mehr
What PROMECON GmbH makes
PROMECON GmbH manufactures single-use infusion bags (CareVis Bag I/L, CareVis Bag S/M, CareVis Bag X/G) and associated infusion sets (CareVis Set) for intravenous administration of fluids and medications. These products are designed for clinical use in hospital and outpatient settings, including low-, standard-, and large-volume infusion applications. The company also supplies sterile device covers and reusable high-frequency (HF) surgical instruments, alongside disposable surgical tools. All listed products are intended for one-time use or single-patient procedures.
The company’s infusion bags and sets fall under Class I and Class IIb regulatory classifications in the EU, with all relevant devices registered in the eudamed database. Surgical instruments and device covers are subject to Class I requirements, while infusion-related products may require additional conformity assessments depending on their specific design and risk profile. PROMECON GmbH is headquartered in Germany and adheres to EU Medical Device Regulation (MDR) compliance standards for its portfolio.
Information
- Country
- Germany
- Address
- 10, Kreuslerstraße, Hamburg, Germany
- Website
- www.promecon-medical.com
- [email protected]
- Phone
- +49 40 36 90 16 90
- EUDAMED SRN
- DE-MF-000015290