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Sinus frontal curette,

Spiggle & Theis Medizintechnik GmbH · Model 30-205-70 · UDI-DI 04250676718792

JYG Prescription
7
510(k) clearances
27
Adverse events
1
Recalls
148
Facilities

Description

oblong, 70° curved 18.5 cm

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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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.