Primary Device ID | 00862563003115 |
NIH Device Record Key | 84f9ca93-acae-4329-b4ca-31ac4c502f0a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | inFlow Device |
Version Model Number | March 2017 |
Catalog Number | 203511-45 |
Company DUNS | 005928578 |
Company Name | VESIFLO INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00862563003115 [Primary] |
PIH | Urethral Insert With Pump For Bladder Drainage |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
[00862563003115]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-06 |
Device Publish Date | 2021-08-28 |
00862563003146 | Intraurethral Valve-Pump |
00862563003139 | Intraurethral Valve-Pump |
00862563003122 | Intraurethral Valve-Pump |
00862563003115 | Intraurethral Valve-Pump |
00862563003108 | Intraurethral Valve-Pump |
00862563003092 | Intraurethral Valve-Pump |
00862563003085 | Intraurethral Valve-Pump |