FDA Device Intelligence
HomeHuman Med AG › Biofill Cannula

Biofill Cannula

Human Med AG · Model Single-use, Ø=3.8, L=150, 4H, Rapid, Extraction · UDI-DI 04260170881069

QPB Prescription
1
510(k) clearances
69
Adverse events
1
Recalls
48
Facilities

Description

Biofill Cannula, Ø=3.8mm, 4 Holes, Rapid, L=15cm, Single-use, Extraction

Recalls

DateFirmReason
2024-10-18HUMAN MED AGThe cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spra

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.