Primary Device ID | B1601006B1 |
NIH Device Record Key | 1af60fdc-2afa-462e-8ee6-231f090aa4a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Freedom Syringe |
Version Model Number | 1006-B |
Company DUNS | 151507563 |
Company Name | PROCEDURE PRODUCTS, 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B1601006B1 [Primary] |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
B1601020W1 | Freedom Syringe, 20cc White Plunger |
B1601010B1 | Freedom Syringe, 10cc Blue Plunger |
B1601003G1 | Freedom Syringe, 03cc Green Plunger |
B1601001R1 | Freedom Syringe, 01cc Red Plunger |
B1601006B1 | Freedom Syringe, 6cc Blue Plunger |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FREEDOM SYRINGE 86508107 5057116 Live/Registered |
Bynum, W. Richard 2015-01-20 |