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Connect Medizintechnik GmbH

Austria AT-PR-000026325 Last updated 23 May 2026

Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

What Connect Medizintechnik GmbH makes

Connect Medizintechnik GmbH manufactures medical devices for neonatal and pediatric care, including stillbirth assistance kits, non-invasive ventilation systems like nCPAP and high-flow therapy sets, and breast milk collection systems. Their product range also includes specialized respiratory support generators designed for use in clinical and home settings.

The company’s devices are classified under EU Medical Device Regulations as Class I and Class IIa, with all relevant products listed in the EU’s eudamed registry. The manufacturer is based in Austria.

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 Connect Medizintechnik GmbH manufacture?

Connect Medizintechnik GmbH specializes in medical devices for neonatal and pediatric care. Their product range includes stillbirth assistance kits like the Bridge Stillhilfeset, non-invasive ventilation solutions such as the Infant Flow/Inspire nCPAP/HighFlow Set 3 and Inspire nCPAP Generator-Set, as well as breast milk collection systems like the Kolostrum Sammelset. These devices are designed to support respiratory and neonatal care in clinical and home settings.

Where is Connect Medizintechnik GmbH based?

Connect Medizintechnik GmbH is based in Austria, as indicated by its country designation. The company’s location is relevant for understanding its regulatory context and operational reach within Europe.

Which regulatory registries list Connect Medizintechnik GmbH’s devices?

All of Connect Medizintechnik GmbH’s devices are listed in the EU’s eudamed registry, which is the official database for medical devices under the EU Medical Device Regulations. Listing in eudamed ensures transparency and traceability of devices marketed within the European Economic Area.

How are Connect Medizintechnik GmbH’s devices classified under EU regulations?

Connect Medizintechnik GmbH’s devices are classified under the EU Medical Device Regulations as either Class I or Class IIa. The classification depends on factors like the device’s intended purpose, risk level, and interaction with the body. For example, non-invasive ventilation systems like nCPAP sets are typically Class IIa due to their higher risk profile compared to lower-risk items like breast milk collection kits, which may fall under Class I.

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

Information

Country
Austria(from SRN)
Address
4, Gspanngasse , Mistelbach, Austria
Phone
+43 2572 32400
EUDAMED SRN
AT-PR-000026325