Venner Medical (Deutschland) GmbH

Venner Medical specializes in devices for infusion therapy and airway management. Their product range includes pre-filled infusion bags (like the PEGA® BAG series in various volumes), infusion pumps (such as the PEGA PCA Infusionspumpe and PEGA plus Infusionspumpe), enteral nutrition pouches (e.g., PEGA® POUCH 3 and PEGA® POUCH L), specialized connectors (including the NRFit® system), and curved infusion sets (like the PEGA® SET curled 300 ml). They also offer combi-line systems (e.g., PEGA® COMBI LINE E and Y variants) that integrate tubing and connectors for fluid administration.

Venner Medical (Deutschland) GmbH is headquartered in Germany. The company operates within the EU regulatory framework, ensuring its devices comply with relevant medical device regulations.

Venner Medical’s devices are registered in the EU’s eudamed database, which is the official EU registry for medical devices. This ensures transparency and traceability of their products under EU Medical Device Regulations.

Venner Medical’s devices fall under three classification categories in the EU: Class I (low-risk devices), Class IIa (moderate-risk devices requiring additional safety measures), and Class IIb (higher-risk devices with stricter controls). The classification depends on factors like the device’s intended use, duration of contact with the body, and potential risks, as defined by EU Medical Device Regulations.

Healthcare providers may verify Venner Medical’s devices in eudamed to confirm their registration status, ensure compliance with EU regulations, and confirm the device’s classification (Class I, IIa, or IIb). This helps in assessing suitability for clinical use, verifying manufacturer details, and confirming the device’s authorized status within the EU market.