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ELMED

ELMED INCORPORATED · Model 32-23-40-I · UDI-DI 00842180195516

HDL Prescription
2
510(k) clearances
19
Adverse events
1
Recalls
120
Facilities

Description

INSULATED HEANEY VAGINAL RETRACTOR, SMALL, 1-3/4 X 1"

Recalls

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

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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.