Home › NIHON KOHDEN AMERICA, INC. › BluPRO®

BluPRO®

NIHON KOHDEN AMERICA, INC. · Model TL-271T · UDI-DI 10841983102704

OLV DRT DRG OLT MHX GWQ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 80cm cable

Recalls

Date	Firm	Reason
2018-02-01	Natus Neurology Inc	Potential to be able to import an ambulatory exam for a patient for which the exam was not started.

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 key Read 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.