Primary Device ID | 10840277408348 |
NIH Device Record Key | 08434acf-98ba-48e9-adda-25e08c46bdaf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Visorb Quick |
Version Model Number | VQ391 |
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 | true |
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 | 00840277408341 [Primary] |
GS1 | 10840277408348 [Package] Contains: 00840277408341 Package: [12 Units] In Commercial Distribution |
GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-21 |
Device Publish Date | 2025-03-13 |
10840277407860 | Suture |
10840277408799 | Suture |
10840277408782 | Suture |
10840277408775 | Suture |
10840277409291 | Suture |
10840277409284 | Suture |
10840277408348 | Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() VISORB QUICK 77155318 3368130 Live/Registered |
CP Medical Corporation 2007-04-12 |