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Monitor, Line Isolation
FDA product code DRI · Class 1 · Cardiovascular
128
Registered devices
7
Adverse events
1
Recalls
4
510(k) clearances
Devices with this code
NAMIC — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — NAVILYST MEDICAL, INC.NAMIC — MEDLINE INDUSTRIES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-02-12 | MEDLINE INDUSTRIES, LP - Northfield | The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway. |
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