Primary Device ID | 10812444026730 |
NIH Device Record Key | d5d64c58-49d5-4908-b15e-4f15ad64b73d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HS SUTURE TAPE |
Version Model Number | HS208 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812444026733 [Primary] |
GS1 | 10812444026730 [Package] Contains: 00812444026733 Package: [6 Units] In Commercial Distribution |
GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2017-07-19 |
00812444027471 | Suture |
10812444026754 | Suture |
10812444026747 | Suture |
10812444026730 | Suture |
10812444026723 | Suture |
10812444026716 | Suture |
10812444026709 | Suture |
20812444024412 | SUTURE |
00810020082074 | Suture |
00810020081923 | Suture |
00810020080834 | Suture |