Primary Device ID | 10812444029441 |
NIH Device Record Key | accbeb93-d4b4-42ca-9da4-fd3f9e617600 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HS FIber |
Version Model Number | HS225 |
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 | 00812444029444 [Primary] |
GS1 | 10812444029441 [Package] Contains: 00812444029444 Package: [6 Units] In Commercial Distribution |
GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-26 |
Device Publish Date | 2024-06-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HS FIBER 85392505 4125447 Live/Registered |
RIVERPOINT MEDICAL, LLC 2011-08-08 |