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CARPEDIEM

BELLCO SRL · Model IB0595580 · UDI-DI 08032979792299

QIR Prescription
1
510(k) clearances
37
Adverse events (3 deaths)
0
Recalls
5
Facilities

Description

BL 250 HEMOFILTRATION/HEMODIALYSIS KIT 025 FOR CARPEDIEM

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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.