Primary Device ID | 10812444024699 |
NIH Device Record Key | 9f72e536-fa65-4452-84e2-56689466bb3e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VILET II QUICK |
Version Model Number | VGQ501C |
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 | 00812444024692 [Primary] |
GS1 | 10812444024699 [Package] Contains: 00812444024692 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 | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2015-12-23 |
10812444025870 | Suture |
10812444025771 | SUTURE |
10812444024699 | SUTURE |
10812444024682 | SUTURE |
10812444024675 | SUTURE |
10812444024668 | SUTURE |
00812444024517 | SUTURE |
10812444024507 | Suture |
10812444024262 | SUTURE |
10812444024255 | SUTURE |
10812444024248 | SUTURE |
10812444024224 | SUTURE |
10812444024217 | SUTURE |
10812444024200 | SUTURE |
10812444024187 | SUTURE |
10812444024170 | SUTURE |
10812444023395 | SUTURE |
10810020083467 | suture |
00810020083453 | suture |
10812444023388 | Suture |
10810020088509 | Suture |
10812444029502 | Suture |
10812444029496 | Suture |
10810020086949 | Suture |
10810020080008 | Suture |