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Para-Pak LV-PVA

MERIDIAN BIOSCIENCE, INC. · Model 900112 · UDI-DI 00840733102448

IFQ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Para-Pak / Para-Pak Ultra based systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation.

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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.