FEFClass II
Tube, Single Lumen, With Mercury Wt Balloon For Intestinal Intubation And / Or Decompression
Gastroenterology, Urology · 21 CFR 876.5980
MDR events33All time
Recalls0All time
Registered firms0Currently listed
510(k) clearances1All time
Recent MDR events
33 adverse event reports on file
- BLAKEMORE TUBEMar 8, 2005MalfunctionBardMW1034871
- RUSCHSep 17, 2001MalfunctionRusch9610520-2001-00164
- BLAKEMORE TUBENov 15, 2000MalfunctionWilly Rusch Ag9610520-2000-00098
- BARD BUTTON DEVICE DECOMPMay 18, 2000MalfunctionBipd Div Cr Bard1223688-2000-00020
- CLAY ADAMS RUBBER CANTOR TUBE, PEDIATRIC SIZE, 12FRNov 10, 1999MalfunctionBecton Dickinson1119779-1999-00006
- SENGSTAKEN TUBESSep 15, 1998MalfunctionRusch Mfg. Uk, Ltd.8010092-1998-00057
- BLAKEMORE TUBEFeb 24, 1998InjuryRusch Mfg. Uk, Ltd.8010092-1998-00005
- MILLER-ABBOTT TUBEJan 21, 1997InjuryWilly Rusch Ag48207-1997-00007
- DAVOLOct 18, 1996InjuryDavol Inc44545
- Unnamed deviceOct 18, 1996Injury1018233-1996-00006
Event type breakdown
Malfunction19
Injury11
Unspecified2
Death1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
0 firms currently registered for this product code
No registered firms found for this product code.
510(k) clearances
1 clearances for this product code