Floseal Matrix is indicated in surgical procedures (other than in ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.
Floseal Hemostatic Matrix - 1503351
Device Description
A bioabsorbable device derived from animal collagen (e.g., bovine or porcine collagen) designed to produce a rapid haemostasis through platelet activation/aggregation (which initiates the haemostatic cascade leading to a fibrin clot) during a surgical procedure. It is applied directly to the wound where it remains to be absorbed by the body; it is not dedicated to a specific anatomy/application and does not contain an antimicrobial agent. It may be supplied as a fibrillar or soft, pliable pad/sponge or loose fibres; it may be applied in combination with fibrin adhesives. This is a single-use device.
Environmental Conditions
- Do Not Freeze
- Keep Dry and away from sunlight
- 25.00
- 2.00
Device Sizes
- Total Volume: 10 Milliliter
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: LMF
Device Name: Agent, Absorbable Hemostatic, Collagen Based
Device Class: 3
Physical State: N/A
Definition: N/A
Submission Type ID: 2
Review Panel: SU
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: Y
Target Area: N/A
Regulation Number: 878.4490
Third Party Flag: N
Medical Specialty: SU
Code: PMX
Device Name: Absorbable Collagen Hemostatic Agent With Thrombin
Device Class: 3
Physical State: collagen plus thrombin
Definition: Intended for use as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.
Submission Type ID: 2
Review Panel: SU
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: Hemostatic agent combining tamponade and acceleration of fibrin clot formation
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: Y
Target Area: Surgical procedures other than ophthalmic
Regulation Number: 878.4490
Third Party Flag: N
Medical Specialty: SU
Device Identifiers
Device Id: 00085412096117
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A