FDA Device Intelligence
HomeRUMEX INTERNATIONAL CORP. › Rumex

Rumex

RUMEX INTERNATIONAL CORP. · Model 14-025S · UDI-DI 00840159902844

HNC
10
510(k) clearances
21
Adverse events
1
Recalls
190
Facilities

Description

Barraquer Wire Speculum, Open 18.00 mm Blades, Adult Size, Length 45 mm, Stainless Steel

Recalls

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

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.