Primary Device ID | 00810020083255 |
NIH Device Record Key | d4c96817-535b-42f5-91a2-4b0c8e9266d4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HS Fiber |
Version Model Number | HS1045 |
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 | 00810020083255 [Primary] |
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 | 2020-04-07 |
Device Publish Date | 2020-03-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HS FIBER 85392505 4125447 Live/Registered |
RIVERPOINT MEDICAL, LLC 2011-08-08 |