SURFLASH safety I.V. catheter
SURFLASH - SR*FNP2032
Device Description
A sterile, thin, flexible tube intended to be inserted into the peripheral vasculature of a patient to enable short-term (< 30 days) intravascular access; it is not intended to be advanced to the central vasculature. It typically includes dedicated accessories to facilitate catheter introduction/placement and function (e.g., connectors, injection ports, stylet and/or wings for fixation). It may be used for blood sampling, monitoring of blood pressure, to administer fluids, medication and/or for the injection of contrast media. This is a single-use device.
Environmental Conditions
- Stacking limit by 5, Keep away from sunlight, Fragile, handle with care, Keep dry
- Do not store at extreme temperature and humidity.
Device Sizes
- Catheter Gauge 20 Gauge
- Length: 1.25 Inch
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: FOZ
Device Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device Class: 2
Physical State: N/A
Definition: N/A
Submission Type ID: 1
Review Panel: HO
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 880.5200
Third Party Flag: Y
Medical Specialty: HO
Device IdentifiersDevice Id: 54987350709863
Device Type: Package
DeviceId Issuing Agency: GS1
Contains DI Number: 34987350709869
Package Quantity: 4
Package Discontinue Date: 8/29/2018 12:00:00 AM
Package Status: Not in Commercial Distribution
Package Type: N/A
Device Id: 34987350709869
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
Device Id: 04987350709868
Device Type: Unit of Use
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