Primary Device ID | 00883489001603 |
NIH Device Record Key | 6fa1fd4c-7203-4df8-871d-14cbe0ff3afe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rightest |
Version Model Number | GC300 |
Company DUNS | 658637244 |
Company Name | BIONIME CORPORATION |
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 | false |
OTC Over-The-Counter | true |
Phone | +1 888 481 8485 |
info@bionime.com |
Total Volume | 4 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883489001603 [Primary] |
JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-04-20 |
00883489310293 | GM250 |
00883489001603 | GC300 |
00883489001498 | GS100 |
20883489001461 | GP200 |
20883489001423 | GS100 |
00883489001405 | GS300 |
20883489001164 | GS550 |
20883489001140 | GM550 |
00883489001078 | GS100 |
20883489001065 | GM100 |
00883489001047 | GC300 |
20883489001034 | GS300 |
00883489001009 | GM300 |
00883489002037 | 25 pcs strips(80883489002033) per vial, 2 vials(00883489002037) per box |
00883489001993 | 1 meter - 00883489001986 1 lancing device - 00883489002013 1 control solution -00883489002020 |
00883489001306 | single lancing device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RIGHTEST 78326886 3077438 Live/Registered |
Bionime Corporation 2003-11-12 |