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Joseph nasal rasp

Spiggle & Theis Medizintechnik GmbH · Model 20-829-17 · UDI-DI 04250676740236

KBA Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities

Description

single ended, coarse 17 cm

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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.