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Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma

FDA product code MDP · Class 3 · Unknown

103
Registered devices
220
Adverse events
3
Recalls
0
510(k) clearances

Devices with this code

Timberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTimberline® MPF Lateral Interbody Modular Plate Fixation System — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLCTIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM — BIOMET SPINE LLC

Recent recalls

DateFirmReason
2026-01-06VANTIVE US HEALTHCARE LLCThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
2014-07-18Gambro Renal Products, IncorporatedGambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.
2014-07-18Gambro Renal Products, IncorporatedGambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.