FDA Device Intelligence
Home › Hermann Medizintechnik GmbH › Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH · Model H50-050-037 · UDI-DI 04059453040756

FFD Prescription
2
510(k) clearances
8
Adverse events
0
Recalls
34
Facilities

Description

Luer-Lock tube connectionwith stopcock

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.