FDA Device Intelligence
HomeRZ-Medizintechnik GmbH › RZ Medizintechnik GmbH

RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 420-150-165 · UDI-DI 04049197311908

KAK Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
92
Facilities

Description

Killian nasal probe Ø1,5mm, slightly curved, 165 mm, 6 1/2"

Recalls

DateFirmReason
2012-08-17Vital Signs Colorado Inc.There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

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.