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House suction cannula, Luer-Lock

Spiggle & Theis Medizintechnik GmbH · Model 10-308-10 · UDI-DI 04250381801901

JZF Prescription

510(k) clearances

Adverse events

Recalls

145

Facilities

Description

7 cm, 1.0 mm

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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.