Primary Device ID | 00857136004163 |
NIH Device Record Key | fd9f42ae-6e2e-4361-afad-d7507d0326f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surefire Spark Infusion System |
Version Model Number | SPARK-A150 |
Company DUNS | 832575497 |
Company Name | SUREFIRE MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Lumen/Inner Diameter | 0.021 Inch |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Length | 150 Centimeter |
Lumen/Inner Diameter | 0.021 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857136004163 [Primary] |
DQO | Catheter, Intravascular, Diagnostic |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
[00857136004163]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-09 |
Device Publish Date | 2018-05-04 |
00857136004163 | 150cm 0.021" Microcatheter w/ 1.5-3.5mm Expandable Tip |
00857136004187 | 120cm 0.021" Microcatheter w/ 1.5-3.5mm Expandable Tip |