Primary Device ID | 10812444024705 |
NIH Device Record Key | b608cdf7-d055-4958-b7a4-42feb3072826 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MONO Q |
Version Model Number | Q493C |
Company DUNS | 964053560 |
Company Name | RIVERPOINT MEDICAL, LLC |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812444024708 [Primary] |
GS1 | 10812444024705 [Package] Contains: 00812444024708 Package: [12 Units] In Commercial Distribution |
GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-12-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MONO Q 86510082 4777286 Live/Registered |
GE HEALTHCARE BIOPROCESS R&D AB 2015-01-21 |
![]() MONO Q 85392445 4114963 Live/Registered |
RIVERPOINT MEDICAL, LLC 2011-08-08 |
![]() MONO Q 73462558 1311779 Live/Registered |
Pharmacia AB 1984-01-24 |