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Healeon HD PRP

Bimini Technologies LLC · Model HDPRP15 · UDI-DI 00850034511313

ORG Prescription
0
510(k) clearances
432
Adverse events
0
Recalls
106
Facilities

Description

A sterile, single use, polyester gel media containing, vacuum evacuated tube that is intended for separating and concentrating blood components along with the use of a desktop centrifuge.

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

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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.